Gray B - Search Results

1

Zori RT, Hendrickson J, Woolven S, Whidden EM, Gray B, Williams CA. Zori RT, et al. Among authors: gray b. J Child Neurol. 1992 Jul;7(3):270-80. doi: 10.1177/088307389200700307. J Child Neurol. 1992. PMID: 1634750 Review.

2

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

3

Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.

Williams CA, Gray BA, Hendrickson JE, Stone JW, Cantú ES. Williams CA, et al. Among authors: gray ba. Am J Med Genet. 1989 Mar;32(3):339-45. doi: 10.1002/ajmg.1320320313. Am J Med Genet. 1989. PMID: 2786338

4

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

5

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. Among authors: gray b. 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

6

Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-like phenotype.

Stalker HJ, Keller KL, Gray BA, Zori RT. Stalker HJ, et al. Am J Med Genet A. 2003 Jan 15;116A(2):176-8. doi: 10.1002/ajmg.a.10001. Am J Med Genet A. 2003. PMID: 12494438

7

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.

8

Smith-Lemli-Opitz syndrome in a female with a de novo, balanced translocation involving 7q32: probable disruption of an SLOS gene.

Wallace M, Zori RT, Alley T, Whidden E, Gray BA, Williams CA. Wallace M, et al. Among authors: gray ba. Am J Med Genet. 1994 May 1;50(4):368-74. doi: 10.1002/ajmg.1320500414. Am J Med Genet. 1994. PMID: 8209918

9

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion.

Zori RT, Lupski JR, Heju Z, Greenberg F, Killian JM, Gray BA, Driscoll DJ, Patel PI, Zackowski JL. Zori RT, et al. Among authors: gray ba. Am J Med Genet. 1993 Sep 15;47(4):504-11. doi: 10.1002/ajmg.1320470414. Am J Med Genet. 1993. PMID: 8256814

10

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

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