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| Mazin B. Qumsiyeh (PhD)
- Born in 1957 in Beit
Sahour, a suburb of Bethlehem in the area now occupied by Israel since 1967. He is married
with one son (now enrolling at MIT).
- Published over 100 letters
to the editor and 30 op-ed pieces in International, national, regional and local papers on issues
ranging from politics to environmental issues. Personal web page: http://info.med.yale.edu/genetics/fac/MazinQumsiyeh.htm
Peer Reviewed Original Research Qumsiyeh,
M. B. New records of bats from Jordan.Säugetierk.
Mitt. 1980, 28(1): 36-39. Qumsiyeh,
M. B. and D. A. Schlitter. Bat records from Mauritania,
Africa (Mammalia: Chiroptera). Annals of the Carnegie Museum of Natural History, 1981,
50(13):345-351. Qumsiyeh,
M. B. and D. A. Schlitter. The bat fauna of Jabal al
Akhdar, North East Libya. Annals of the Carnegie Museum of Natural History, 1982,
51(19):377-389. Qumsiyeh,
M. B. Occurrence and zoogeographical implications of Myotis
blythi (Tomes, 1857) in Libya. Mammalia (Paris), 1983, 47(3):429-430. Qumsiyeh,
M. B. and R. J. Baker. G- and C-banded karyotypes of the Rhinopomatidae (Microchiroptera). Journal
of Mammalogy, 1985, 66:541-544. Qumsiyeh,
M. B. Phylogenetic studies of the rodent family
Gerbillidae: I. Chromosomal evolution in the southern
African group. Journal of Mammalogy, 1986,
67:680-692. Qumsiyeh,
M. B., D. A. Schlitter, and A. M. Disi. New records and
karyotypes of small mammals from Jordan. Zeitschrift für Säugetierkunde, 1986, 51:139-146. Schlitter,
D. A., I. R. Aggundey, M. B. Qumsiyeh, K. Nelson, and R. L. Honeycutt. Taxonomic and distributional
records on bats from Kenya. Annals of the Carnegie Museum of Natural History, 1986,
55(12):297-302. Qumsiyeh,
M. B., M. J. Hamilton, and D. A. Schlitter. Problems of
using Robertsonian rearrangements in determining monophyly: examples from the genera Tatera
and Gerbillurus.Cytogenetics and Cell Genetics, 1987, 44:198-208. Owen,
R. D. and M. B. Qumsiyeh. The subspecies problem in the
trident leaf-nosed bat, Asellia tridens: homomorphism in widely separated populations.
Zeitschrift für Säugetierkunde, 1987, 6:329-337. Qumsiyeh,
M. B. and R. K. Chesser. Rates of protein, chromosome,
and morphologic evolution in four genera of Rhombomyine gerbils. Biochemical Systematics and
Ecology, 1988, 16(1):89-103. Qumsiyeh,
M. B. Pattern of heterochromatic variation and
phylogeny in the rodent family Gerbillidae. Texas Journal of Science, 1988,
40:63-70. Qumsiyeh,
M. B., R. J. Baker, S. Davis, J. C. Patton, and C. S. Hernandez.
Chromosomal evolution in Geomys as revealed by G- and C-band studies.
Southwestern Naturalist , 1988,
33(1):1-13. Qumsiyeh,
M. B., R. D. Owen, and R. K. Chesser. Differential
rates of protein and chromosome evolution in bats of the family Rhinolophidae.Genome, 1988,
30:326-335. Baker,
R. J., M. B. Qumsiyeh, and I. L. Rautenbach. Evidence
for eight tandem and five centric fusions in the karyotype of Aethomys namaquensis. Genetica,
1988, 76:161-169. Qumsiyeh,
M. B., M. B. Valentine, and D. P. Suttle. Localization of the gene for uridine monophosphate
synthase to human chromosome region 3q13 by in situ hybridization. Genomics,
1989, 5:160-162. Qumsiyeh,
M. B. Chromosomal fissions and phylogenetic hypotheses: Cytogenetic and allozymic variation between
species of Meriones (Rodentia, Gerbillidae).Occasional Papers of the Musuem, Texas Tech
Univ., 1989, 132:1-16. Qumsiyeh,
M. B. and D. P. Suttle. Cytogenetic analysis of amplification and deamplification of UMP synthase
gene in Chinese hamster cells. Somatic Cell and
Molecular Genetics, 1989, 15:503-512. Qumsiyeh,
M. B., S.W. King, J. Arroyo-Cabrales, I. R. Aggundey, D. A. Schlitter, R. J. Baker, and K.J. Morrow.
Complex chromosomal and immunological evolution in the morphologically similar species
of murid rodents of the Mastomys/Praomys Complex. Journal of Heredity, 1990, 81(1):58-65. Qumsiyeh,
M. B. and D. P. Suttle. Localization of the adenosine deaminase, transferrin, and UMP synthetase
genes on Chinese hamster chromosomes 4 and 6 by
in situ hybridization. Journal of Heredity, 1990,
81(2):111-116. Pivnick,
E. K., M. B. Qumsiyeh, A. T. Tharapel, J. B. Summitt, R. S. Wilroy. Partial duplication of the long
arm of chromosome 6: a clinically recognizable syndrome. Journal of Medical Genetics, 1990,
27:523-526. Qumsiyeh,
M. B., A. T. Tharapel, L. P. Shulman, S. E. Elias, and J. L. Simpson. Anaphase lag as the most
likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from
the same villi. Journal of Medical Genetics, 1990, 27:780-781. Qumsiyeh,
M. B., J. N. Peeden, R. S. Wilroy, and A. T. Tharapel. High resolution replication banding combined
with in situ hybridization for the delineation of a subtle
chromosome rearrangement. American Journal of Medical Genetics. 1991, 41:99-101. Qumsiyeh,
M.B., E. D. Dempster, M. J. Hamilton and R. J. Baker. Cytogenetics and systematics of the rodent
genus Gerbillurus. Journal of Mammalogy, 1991, 72(1):89-96. Tharapel,
A. T., M. B. Qumsiyeh, P. R. Martens, S. A. Tharapel, J. D. Dalton, J. C. Ward, and R. S. Wilroy.
Identification of the origins of centromeres in whole-arm translocations using fluorescent in
situ hybridization with alpha satellite DNA probes. American Journal of Medical Genetics.
1991, 40: 117-120. Tharapel,
S. A., M. B. Qumsiyeh, and G. Photopulos. Numerical chromosome abnormalities associated with early
clinical stages of gynecologic tumors. Cancer Genetics and Cytogenetics. 1991, 55:89-96. Qumsiyeh,
M. B. Karyotype of the East European hedgehog, Erinaceus concolor from
Jordan. Zeitschrift für Säugetierkundliche.
1991, 56:375-377. Qumsiyeh,
M. B. Letter to the editor. Perspectives in Biology and Medicine 1991, 34(4):468-469. Qumsiyeh,
M. B., J. D. Dalton, P. L. Gordon, R. S. Wilroy, and A.
T. Tharapel. Deletion of chromosome 15pter®q11.2 due to t(Y;15) in a boy with Prader-Willi
syndrome. American Journal of Medical Genetics 1992,
42:109-111. Qumsiyeh,
M. B., J. D. Dalton, P. L. Gordon, R. S. Wilroy, and A.
T. Tharapel. Response to Zelante et al. American Journal of Medical Genetics. 1992, 44:846. Qumsiyeh,
M. B. and S. A. Tharapel. Detection of trisomy 12 in chronic lymphocytic leukemia using fluorescence
in situ hybridization. Leukemia. 1992, 6(6): 602-605. Qumsiyeh,
M. B., Z. S. Amr, and A. M. Disi. Systematics and
distribution of the bats (Mammalia: Chiroptera) of Jordan. Dirasat (Jordan Univ. Publications). 1992,
9B(2):101-118. Qumsiyeh,
M. B. S. Goorha, and D. P. Suttle. Gene amplification and chromosome rearrangements: a study of a
single cell lineage selected for amplification and deamplification of the UMP synthase gene. Cytogenetics
Cell Genet., 1993, 62:162-168. Qumsiyeh,
M. B., Z. S. Amr, and D. M. Shafi. Status and
conservation of the carnivores of Jordan (Mammalia: Carnivora). Mammalia. 1993, 57(1):55-62. Amr,
Z. S. and Qumsiyeh, M. B. Records of bat flies from
Jordan, Libya, and Algeria. Entomological News. 1993, 104(1):43-46. Qumsiyeh,
M. B., and C. A. Stevens. Two siblings with different
phenotypes due to adjacent-1 segregation of a submicroscopic translocation t(4;5)(p16.3;p15.31)mat. Am.
J. Med. Genet. 1993, 47:387-391. Qumsiyeh,
M. B. Distal limb anomalies, Robin sequence and deletions in 4q31-->qter (letter to the editor). Am.
J. Med. Genet. 1993, 49:255. Qumsiyeh,
M. B. and J. W. Bickham. Chromosomes and relationships of long eared bats of the genera Plecotus
and Otonycteris. Journal of Mammalogy. 1993,
74(2):376-382. Benkhalifa,
M., P. Malet, M. B. Qumsiyeh, D. Boucher, V. Belliec, Y. Menzo. Chromosome aberrations in normal and
translocated human sperm: role in reproduction pathology. Referens. Geneo. Obstet. 1994,
2(3):288-296. Johnson,
D. W., M. B. Qumsiyeh, M. Benkhalifa, and D. Marchuk. Assignment of human transforming growth factor
b type I and type III receptor genes (TGFbR1 and TGFbR3) to 1p32-33 and 9q33q34. Genomics,
1995, 28:356-357. Taiar,
N., M. B. Qumsiyeh, J. Poulet, M. Benkhalifa. Delineation
of translocation X;Y using DNA probes. Ann. Genet. 1995,
38(2):102-105. Stevens,
C. A. and M. B. Qumsiyeh. Syndromal frontonasal dysostosis in a child with a complex translocation
involving chromosomes 3, 7, and 11. Am. J. Med. Genet. 1995, 55:494-497. Teebi,
A. S., M. B. Qumsiyeh, C. H. Meyers-Seifer, M. S. Neyn.
Velo-facio-skeletal syndrome in a mother and daughter. Am.
J. Med. Genet. 1995, 58: 8-12. Qumsiyeh,
M. B., A. Tomasi, and M. M. Taslimi. Short arm deletion
and isochromosome 18 formation detected at amniocentesis.J. Med Genet. 1995, 32(12):991-993. Helali,
A. N., A. K. Iafolla, and M. B. Qumsiyeh. A case of duplication of 13q32-->qter with mild
phenotype: Patau syndrome and duplications of 13q revisited. J. Med. Genet. 1996, 33:600-602. Qumsiyeh,
M. B. and J. A. Peppers. Sensitivity and specificity of whole chromosome paint (WCP) probes are
correlated with the size of translocated segments. Am. J. Med. Genet., 1996, 65:173. Benkhalifa,
M., Y. Menezo, L. Janny, J. L. Pouly, and M. B. Qumsiyeh. Cytogenetics of uncleaved oocytes and
arrested zygotes in IVF programs. J. Assisted Repr.
& Genetics. 1996, 13(2):140-148. Qumsiyeh,
M. B., J. L. Coate, J. A. Peppers, P. K. Kennedy, M. L. Kennedy. Robertsonian chromosomal
rearrangements in the short-tailed shrew, Blarina carolinensis in western Tennessee. Cytogenet
Cell Genet. 1997, 76:153-158. DeCastro,
C. M., S. M. Rabe, S. D. Langdon, D. E. Fleenor, M. N. Ahmed, M. B. Qumsiyeh, R. E. Kaufman.
Genomic structure and chromosomal localization of PE-2 (ERF), a novel ETS factor with
potential tumor suppressor properties.Genomics., 1997, 42:200-207 Byrd,
J.C., R. W. Weiss, D. C. Arthur, D. Shah, M. R. Baer, D. Laurence, F. Davey, E. S. Trikha, A. J.
Carroll. R. Tantavahi, and M. B. Qumsiyeh. S. R. Patil, J. Moore, R. J. Mayer, C. A. Scjiffer, C. D.
Bloomfield. Extramedullary leukemia adversely affects hematologic complete remission rate and
overall survival in patients with t(8;21)(q22;q22): Results from CALGB 8461. J Clin Oncology
. 1997, 15(2):466-475. Hinson,T.,
T. V. Damodaran, X. X. Chang, M. B. Qumsiyeh, M. F. Seldin, and D. L. Quarles.
Identification of putative transmembrane receptors homologous to the calcium sensing
G-coupled receptor. Genomics. 1997, 45:279-289. Qumsiyeh,
M. B., Adhvaryu, S. G., L. Fry-Mehltretter, T. Peters-Brown, and Helen Kay. Discrepancies in cytogenetic findings in chorionic villi. J. Maternal Fetal
Medicine, 1997, 6:351-355. Adhvaryu,
S. G., M. Decker-Phillips, Trisha Peters-Brown, E. Livingstone, and M. B. Qumsiyeh.
Marker chromosome evolution in a three generation family. Prenatal Diagnosis, 1998,
118:178-181. Liao,
M-J, X-X Zhang, M. B. Qumsiyeh, and T. Van Dyke. No
role for V(D)J recombination in p53-deficient thymic lymphoma. Mol. Cellular Biol. 1998, 18(6):3495-3501. Qumsiyeh,
M. B. Chromosome abnormalities in the placenta and
spontaneous abortions. J. Matern.-Fetal Med. 1998, 7:210-212. Heinonen,
K., K. Mrozek, D. Lawrence, D. C. Arthur, M. J. Pettenati, J. Stamberg, M. B. Qumsiyeh, R. S. Verma,
J. MacCallum, C. A. Schiffer, C. D. Bloomfield. Clinical characteristicsof patients with de novo
acute myeloid leukemia and isolated trisomy 11: Cancer and leukemia group B study 8461. Br. J.
Haematol. 1998, 101-513-520. Ahmed,
M. N., A. P. Killam, K. Thompson, and M. B. Qumsiyeh. Unconjugated estriol as an indication for
prenatal diagnosis of steroid sulfatase deficiency by in situ hybridization. Obstetrics &
Gynecology. 1998, 92:687-689. Qumsiyeh,
M. B. , Z. S. Amr, R. M. Al-Oran. Further records of bats from Jordan and a synopsis. Turkish J.
Zoology. 1998, 22:277-284. Klintworth,
G. K., J. Sommer, L. Han, L., G. OBrian, M. N. Ahmed, M. B. Qumsiyeh, et al. Familial subepithelial
corneal amyloidosis (gelatinous drop-like corneal dystrophy): Exclusion of linkage to lactoferrin
gene. Molecular Vision 1998, 4:31 (www.molvis.org/molvis/v4/p31). Byrd,
J.C., D. Laurence, D. C. Arthur, M. J. Pettenati, R. Tantavahi, M. B. Qumsiyeh, J. Stamburg, F.
Davey, C. A. Schiffer, C. D. Bloomfield. Patients with isolated trisomy 8 in acute myeloid leukemia
are not cured with cytarabine-based chemotherapy: Results from CALGB 8461. Clinical Cancer
Research 1998, 4(5):1235-1241. Ashley-Koch,
A., C.M. Wolpert, L. Zaeem, M. M. Menold, M. B. Qumsiyeh et al. Genetic studies of autistic
disorders and chromosome 7. Genomics. 1999, 61:227-236. Qumsiyeh,
M.B., S. Barker, S. Dover,
P. K. Kennedy, and M. P. Kennedy. A potential model for early stages of chromosomal evolution
by concentric Robertsonian fans: a large area of polymorphism in southern short-tailed shrews (Blarina
carolinensis). Cytogenet. Cell Genet. 1999, 87(1-2):27-31 Curotti,
G., M. Benkhalifa, C. Raybaud, F. Picard, V. Belec, M. B. Qumsiyeh. De novo highly complex
chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by
FISH. Genetic Counseling. 1999, 10:259-264. Zhang,
XX, L. J. Robinson, T. T. Stenzel, and M. B. Qumsiyeh. Translocation
t(15;17)(q22;q12-21) as a secondary chromosomal abnormality in a case of acute monoblastic leukemia
with tetrasomy 8. Cancer Genet Cytogenet. 1999, 113:9-13. Qumsiyeh,
M.B., C. Cheng, J. Eyre, K. P. Mann, and X-X Zhang. Tetrasomy 8 evolving into a translocation
triplication 8q in a case of acute monocytic leukemia. Cancer Genet & Cytogenet. 1999,
116:10-15. Powell,
J., T. Traweek, M. B. Qumsiyeh, and P. M. Rosoff. A novel chromosomal rearrangement associated with
therapy-related acute leukemia. Cancer Genet Cytogenet 1999, 112:173-177. Byrd,
J.C., R. Dodge, A. Carroll, M. Baer, C. Edwards, J. Stamburg, M. B. Qumsiyeh, J. O. Moore, R. J.
Mayer, R. Larson, C. D. Bloomfield. Patients with t(8;21)(q22;q22) and acute myeloid leukemia have a
superior disease free and overall survival when repetitive cycles of high-dose cytarabine are
administered: Results from CALGB 8461. J Clin Oncology. 1999, 17:3767-3775. Shen,
J.J., D. Mattern, D. S. Millington, S. Hillman, M. D. Feezor, M. J. Bennett, M. B. Qumsiyeh, S. G.
Kahler, Y.-T. Chen, and J. L. K. VanHove. Acylcarnitine produced in vitro by cultured fibroblasts of
patients with long-chain 3-hydroxyacylcoenzyme A dehydrogenase deficiency and other disorders of
fatty acid oxidation. Journal of Inherited Metabolic Disease. 2000, 23(1):27-44. Ahmad,
M. N., K. Kim, B. Haddad, A. Berchuck, M. B. Qumsiyeh.
Comparative genomic hybridization studies in hydatidiform moles and choriocarcinoma: Amplification
of 7q21-q31 and loss of 8p12-p21 in choriocarcinoma. Cancer Genet Cytogenet 2000, 116:10-15. Melvin,
E.C., T. George, G. Worley, A. Franklin, J. Mackey, K. Viles, N. Shah, C. R. Drake, D. McLone, J.
Nye, J. Oakes, C. McLaaughlin, M. L. Walker, P. Peterson, T. Brei, C. Buran, J. Aben,
M.B. Qumsiyeh, J. Vance, M.A. Pericack-Vance, M. C. Speer, and the NTD Collaborative Group.
Genetic studies of neural tube defects. Pediatr Neurosurg. 2000, 32(1):1-9. Ahmed,
M. N., G. R. DeLong, and M. B. Qumsiyeh. Postnatal
Developmental delay (PNDD) and chromosome abnormalities. Clinical Pediatrics 2000,
39:233-235. Sen,
F., V. Prieto, C. Shea, and M. B. Qumsiyeh. Increased
incidence of trisomy 8 in AML with skin infiltration: use of FISH in diagnosis of leukemia cutis. Diagnostic
Molecular Pathology 2000, 9(4):190-194. Wolpert,
C. M., M. M. Menold, M. P. Bass, M. B. Qumsiyeh, S. L. Donneely, S. Ravan, R. Abramson, H. Wright,
L. O. Maddox, J. M. Vance, J. R. Gilbert, M. L. Cuccaro, and M. A. Peroicak-Vance. Three patients
with autistic disorder and isodicentric chromosome 15. . Am J Med Genetics. 2000, 96(3):
365-372 Qumsiyeh,
M. B., K-R. Kim, W. Bradford. Cytogenetics and mechanisms of spontaneous abortions:
Increased apoptosis and decreased cellular proliferation in chromosomally abnormal villi. Cytogenet
Cell Genet 2000, 88(3-4):230-235. Rafi,
S., H. ElGebaly, and M. B. Qumsiyeh. A high incidence of TEL/AML1 fusions accompanying other
chromosome abnormalities in childhood B-precursor ALL. Diagnostic Molecular Pathology 2000,
9(4):184-189. Henegariu
O, Bray-Ward P, Artan S, Vance GH, Qumsyieh M, Ward DC. Small marker chromosome identification in
metaphase and interphase using centromeric multiplex fish (CM-FISH). Lab Invest. 2001, 81(4):475-81. Smith
DS. Leone G. DeGregori J. Ahmed MN. Qumsiyeh MB. Nevins JR. Induction of DNA replication in adult
rat neurons by deregulation of the retinoblastoma/E2F G1 cell cycle pathway. Cell Growth &
Differentiation. 2000, 11(12):625-33. Kone
J, Chen W, Savinelli T, Arroyo J, Boyd K, Buchberg A, Wu Y, Nimmakayalu M, Copeland N, Jenkins N,
Qumsiyeh M, Hu P, Prescott A, Wu H, Yang L, Roe B, Perkins A. F-MuLV Acceleration of myelomonocytic
tumorigenesis in SV40 T antigen transgenic mice is accompanied by retroviral insertion at Fli1 and a
novel locus, Fim-4. Leukemia. 2002; 16:1827-1834. Qumsiyeh,
MB., S Rafi, C Sarri, M Grigoriadou, J Gyftodimou, E Pandelia, H Laskari , M B Petersen.
Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy.
Am J Med Genet. 2003, 116A:356-359. Hui,
P., J. G. Howe, J. Crouch, M. Nimmakayalu, M. B. Qumsiyeh, G. Tallini, S. D. Flynn, B. R. Smith.
Real-time quantitative RT-PCR of Cyclin D1 mRNA in mantle cell lymphoma: Comparison with FISH and
immunohistochemistry. Leukemia and Lymphoma, 2003, 44(8):1385-1394. Benkhalifa,
M., S. Kahraman, D. Caserta, E. Domez, M. B. Qumsiyeh. Morphological and cytogenetic analysis of
intact oocytes and blocked zygotes. Prenatal Diagnosis, 2003, 23(5):397-404 Yilmaz,
Y., R. Klein, MB Qumsiyeh. Trisomy 6 acquired in lymphoid blast transformation of CML with t(9;22). Cancer
Genet Cytogenet. 145:86-87. Zhang,
P, P Li, D Wang, S Huff, M Nimmakayalu, M Qumsiyeh, B Pober. FOXC1 gene deletion is associated with
eye abnormalities in ring chromosome 6. In press Am J
Med Genet. Benkhalifa
M, S Kahraman, MD A Biricik, S Serteyl, E Domez,Y Kumtepe, M B Qumsiyeh. Cytogenetics and FISH
analysis after round spermatid injection: intact oocytes to day 4 embryos. In press, Fertility and
Sterility. Qumsiyeh,
M.B., Ahmed, M.N., K. Lucas, C. Shea, V. M. Prietto, Amplification of 20q13 and likely
involvement of STK15 locus in development of “dysplastic” nevi and melanoma. Submitted to Melanoma
Research. Ballo,
M.J., Kim, K-R, and M. B. Qumsiyeh. Trisomy of Chromosomes 7, 16, and 17 in Papillary Renal Cell
Neoplasms: Detection in Formalin-Fixed Paraffin-Embedded Sections by Fluorescence In Situ
Hybridization. Submitted to Laboratory
Investigation. Editorials,
Reviews, Chapters (peer reviewed) Qumsiyeh,
M. B. and J. K. Jones, Jr. Rhinopoma hardwickii
and R. muscatellum. Mammalian
Species, American Society of Mammalogists, 1986, 263:1-5. Baker,
R. J., M. B. Qumsiyeh, and C. S. Hood. Role of
chromosomal banding patterns in understanding mammalian evolution.
Pp. 67-96 in Current Mammalogy,
Vol. 1 (H. H. Genoways, ed.), Plenum Publishing Corporation, New York. 1987. Qumsiyeh,
M. B. and R. J. Baker. Comparative cytogenetics and the determination of primitive karyotypes. Cytogenetics
and Cell Genetics, 1988, 47:100-103. Baker,
R. J. and M. B. Qumsiyeh. Methods in chiropteran
mitotic chromosomal studies. Pp. 425-435 In Ecological
and Behavioral Methods for the Study of Bats (T.
H. Kunz, ed.), Smithsonian Inst. Press, Washington DC. 1988. Qumsiyeh,
M. B. On the nature of controversies in evolutionary biology. Perspectives in Biology and
Medicine, 1990, 33(3):421-430. Qumsiyeh,
M. B. and Z. S. Amr. Mammals of Jordan: Rodents. Al-Reem (Royal Society for the Conservation of
Nature). 1991, 44:19-20. [In Arabic]. Qumsiyeh,
M. B. and D. A. Schlitter. Cytogenetic data on the rodent family Gerbillidae. Occasional Papers
of the Museum, Texas Tech University 1991,
144:1-20. Qumsiyeh,
M. B. Review of "Mammals of Arabia" by D. L. Harrison and P. J. Bates. Journal
of Mammalogy 1992, 73(1):228-229. Qumsiyeh,
M. B. Review of "Mammals of Algeria" by K. Kowalski and B. Rzebik-Kowalska.
Journal of Mammalogy. 1992, 73(2):459-460. Qumsiyeh,
M. B. EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7q11.2-q21.3. Clinical
Genetics 1992, 42(2):101. Suttle,
D. P. and M. B. Qumsiyeh. A reversible selection system for UMP synthase gene amplification and
deamplification. Pp. 255-264 in R. Kellem (ed.)Gene
Amplification in Mammalian Cells: Techniques and Applications . Marcel Dekker Inc., New York,
NY, 543 pp. 1992. Qumsiyeh,
M. B. Evolution of number and morphology of mammalian
chromosomes. J. Heredity. 1994, 85:455-465. Gharaibeh,
B. and M. B. Qumsiyeh. Otonycteris hemprichii. Mammalian Species, American Society of
Mammalogists. No. 514, pp. 1-4. Qumsiyeh,
M. B. Impact of rearrangements on function and position
of chromosomes in the interphase nucleus and on human genetic disorders. Chromosome Research, 1995,
3:455-465. Schlitter,
D. A. and M. B. Qumsiyeh. Rhinopoma microphyllum. Mammalian
Species, American Society of Mammalogists. 1996, No 542, pp. 1-5, 4 figs. Qumsiyeh,
M. B. , Z. S. Amr, A. M. Budari. Status and conservation of Artiodactyla (Mammalia) in Jordan. Mammalia
1996, 60:417-430. Qumsiyeh,
M. B., M. Dasouki, and A. Teebi. Genetics of
Palestinians and Jordanians. pp. 227-258 in "Genetic Disorders Among The Arabs" edited by
Ahmad S. Teebi and T. A. Farag, Oxford Monographs in Genetics No. 33, Oxford Univ. Press. 1997. Qumsiyeh,
M. B. Organization and management of a cytogenetic laboratory in the twenty-first century.
Archives De l’Institute Pasteur Tunis, 1997, LXXIV (3/4): 26-27. Fathallah,
D. M., K. Dellagi, M. B. Qumsiyeh, and A. S. Teebi. Recent advances in molecular genetics of the
Maghreb and the Middle East populations: The first Middle East Genetics Association of America
(MEGA) conference. Am. J. Med. Genet. 1998, 78:90-91. Qumsiyeh,
M. B. Review of “Pathology of the Placenta” Third Edition by Benirschke and Kaufmann, Springer-Verlag,
Int. J. Gynecol. Pathol. 1998, 17:93-94. Qumsiyeh,
M. B. Structure and function of the nucleus: anatomy and physiology of chromatin. Cellular Mol.
Life Sci. (CMLS) 1999, 55:1129-1140. Qumsiyeh,
M. B. S. G. Adhvaryu, and A. Teebi. Cytogenetics.
Pp.20-32 in "Textbook of Clinical Pediatrics," A.Y.
Elzouki, H. A. Harfi, H. M. Nazer, Lippincott, Williams, and Wilkins, 2001. Qumsiyeh,
MB and Peining Li. Molecular Biology of Cancer:
Cytogenetics. Pp. 77-90. In “Cancer: Principles and
Practice of Oncology” V. T. DeVita, Jr, S. Hellman, S. A. Rosenberg (eds). Philadelphia:
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