Qumsiyeh MB - Search Results

1

Three probands with autistic disorder and isodicentric chromosome 15.

Wolpert CM, Menold MM, Bass MP, Qumsiyeh MB, Donnelly SL, Ravan SA, Vance JM, Gilbert JR, Abramson RK, Wright HH, Cuccaro ML, Pericak-Vance MA. Wolpert CM, et al. Among authors: qumsiyeh mb. Am J Med Genet. 2000 Jun 12;96(3):365-72. doi: 10.1002/1096-8628(20000612)96:3<365::aid-ajmg25>3.0.co;2-x. Am J Med Genet. 2000. PMID: 10898916 Review.

2

Genetic studies of autistic disorder and chromosome 7.

Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Aylsworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Ashley-Koch A, et al. Among authors: qumsiyeh mb. Genomics. 1999 Nov 1;61(3):227-36. doi: 10.1006/geno.1999.5968. Genomics. 1999. PMID: 10552924

3

Genetic studies in neural tube defects. NTD Collaborative Group.

Melvin EC, George TM, Worley G, Franklin A, Mackey J, Viles K, Shah N, Drake CR, Enterline DS, McLone D, Nye J, Oakes WJ, McLaughlin C, Walker ML, Peterson P, Brei T, Buran C, Aben J, Ohm B, Bermans I, Qumsiyeh M, Vance J, Pericak-Vance MA, Speer MC. Melvin EC, et al. Pediatr Neurosurg. 2000 Jan;32(1):1-9. doi: 10.1159/000028889. Pediatr Neurosurg. 2000. PMID: 10765131 Review.

4

Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques.

Qumsiyeh MB, Tomasi A, Taslimi M. Qumsiyeh MB, et al. J Med Genet. 1995 Dec;32(12):991-3. doi: 10.1136/jmg.32.12.991. J Med Genet. 1995. PMID: 8825933 Free PMC article.

5

A case of duplication of 13q32-->qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisited.

Helali N, Iafolla AK, Kahler SG, Qumsiyeh MB. Helali N, et al. Among authors: qumsiyeh mb. J Med Genet. 1996 Jul;33(7):600-2. doi: 10.1136/jmg.33.7.600. J Med Genet. 1996. PMID: 8818949 Free PMC article.

6

Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy.

Qumsiyeh MB, Rafi SK, Sarri C, Grigoriadou M, Gyftodimou J, Pandelia E, Laskari H, Petersen MB. Qumsiyeh MB, et al. Am J Med Genet A. 2003 Feb 1;116A(4):356-9. doi: 10.1002/ajmg.a.10050. Am J Med Genet A. 2003. PMID: 12522791

7

Familial supernumerary marker chromosome evolution through three generations.

Adhvaryu SG, Peters-Brown T, Livingston E, Qumsiyeh MB. Adhvaryu SG, et al. Among authors: qumsiyeh mb. Prenat Diagn. 1998 Feb;18(2):178-81. doi: 10.1002/(sici)1097-0223(199802)18:2<178::aid-pd233>3.0.co;2-g. Prenat Diagn. 1998. PMID: 9516020

8

FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6.

Zhang HZ, Li P, Wang D, Huff S, Nimmakayalu M, Qumsiyeh M, Pober BR. Zhang HZ, et al. Am J Med Genet A. 2004 Jan 30;124A(3):280-7. doi: 10.1002/ajmg.a.20413. Am J Med Genet A. 2004. PMID: 14708101 Review.

9

Velo-facio-skeletal syndrome in a mother and daughter.

Teebi AS, Qumsiyeh MB, Meyers-Seifer CH, Meyn MS. Teebi AS, et al. Among authors: qumsiyeh mb. Am J Med Genet. 1995 Jul 31;58(1):8-12. doi: 10.1002/ajmg.1320580103. Am J Med Genet. 1995. PMID: 7573161

10

Tetrasomy 8 evolving into a segmental triplication 8q in a case of acute monocytic leukemia.

Qumsiyeh MB, Cheng C, Eyre J, Mann KP, Zhang XX. Qumsiyeh MB, et al. Cancer Genet Cytogenet. 2000 Jan 1;116(1):74-6. doi: 10.1016/s0165-4608(99)00091-6. Cancer Genet Cytogenet. 2000. PMID: 10616537

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