Gray BA - Search Results

1

Translocation (X;20)(q13.1;q13.3) as a primary chromosomal finding in two patients with myelocytic disorders.

Gray BA, Cornfield D, Bent-Williams A, Zori RT. Gray BA, et al. Cancer Genet Cytogenet. 2003 Mar;141(2):169-74. doi: 10.1016/s0165-4608(02)00764-1. Cancer Genet Cytogenet. 2003. PMID: 12606138

2

Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: prenatal and postnatal late replication studies.

Zori RT, Gray BA, Bent-Williams A, Driscoll DJ, Williams CA, Zackowski JL. Zori RT, et al. Among authors: gray ba. Am J Med Genet. 1993 Jun 1;46(4):379-83. doi: 10.1002/ajmg.1320460407. Am J Med Genet. 1993. PMID: 8357008

3

Fluorescence in situ hybridization assessment of the telomeric regions of jumping translocations in a case of aggressive B-cell non-Hodgkin lymphoma.

Gray BA, Bent-Williams A, Wadsworth J, Maiese RL, Bhatia A, Zori RT. Gray BA, et al. Cancer Genet Cytogenet. 1997 Oct 1;98(1):20-7. doi: 10.1016/s0165-4608(96)00409-8. Cancer Genet Cytogenet. 1997. PMID: 9309114

4

Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency.

Zori RT, Boyar FZ, Williams WN, Gray BA, Bent-Williams A, Stalker HJ, Rimer LA, Nackashi JA, Driscoll DJ, Rasmussen SA, Dixon-Wood V, Williams CA. Zori RT, et al. Among authors: gray ba. Am J Med Genet. 1998 Apr 28;77(1):8-11. Am J Med Genet. 1998. PMID: 9557885

5

A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX.

Gray BA, Bent-Williams A, Wolff DJ, Zori RT. Gray BA, et al. Clin Genet. 2001 Jul;60(1):73-6. doi: 10.1034/j.1399-0004.2001.600112.x. Clin Genet. 2001. PMID: 11531974

6

Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders.

Keller K, Williams C, Wharton P, Paulk M, Bent-Williams A, Gray B, Ward A, Stalker H, Wallace M, Carter R, Zori R. Keller K, et al. Am J Med Genet A. 2003 Mar 1;117A(2):105-11. doi: 10.1002/ajmg.a.10042. Am J Med Genet A. 2003. PMID: 12567405

7

G-banded karyotype and ideogram for the North Atlantic right whale (Eubalaena glacialis).

Pause KC, Bonde RK, McGuire PM, Zori RT, Gray BA. Pause KC, et al. Among authors: gray ba. J Hered. 2006 May-Jun;97(3):303-6. doi: 10.1093/jhered/esj033. Epub 2006 Apr 5. J Hered. 2006. PMID: 16598035

8

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

Williams CA, Zori RT, Stone JW, Gray BA, Cantu ES, Ostrer H. Williams CA, et al. Among authors: gray ba. Am J Med Genet. 1990 Mar;35(3):350-3. doi: 10.1002/ajmg.1320350308. Am J Med Genet. 1990. PMID: 2309781

9

Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient.

Alley TL, Gray BA, Lee SH, Scherer SW, Tsui LC, Tint GS, Williams CA, Zori R, Wallace MR. Alley TL, et al. Among authors: gray ba. Am J Hum Genet. 1995 Jun;56(6):1411-6. Am J Hum Genet. 1995. PMID: 7762564 Free PMC article.

10

Cytogenetic and molecular analysis in Angelman syndrome.

Zackowski JL, Nicholls RD, Gray BA, Bent-Williams A, Gottlieb W, Harris PJ, Waters MF, Driscoll DJ, Zori RT, Williams CA. Zackowski JL, et al. Among authors: gray ba. Am J Med Genet. 1993 Apr 1;46(1):7-11. doi: 10.1002/ajmg.1320460104. Am J Med Genet. 1993. PMID: 8098583

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