Gray BA - Search Results

1

Blood lymphocyte chimerism associated with IVF and monochorionic dizygous twinning: case report.

Williams CA, Wallace MR, Drury KC, Kipersztok S, Edwards RK, Williams RS, Haller MJ, Schatz DA, Silverstein JH, Gray BA, Zori RT. Williams CA, et al. Among authors: gray ba. Hum Reprod. 2004 Dec;19(12):2816-21. doi: 10.1093/humrep/deh533. Epub 2004 Sep 16. Hum Reprod. 2004. PMID: 15375077

2

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.

3

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

4

Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?

Rasmussen SA, Williams CA, Ayoub EM, Sleasman JW, Gray BA, Bent-Williams A, Stalker HJ, Zori RT. Rasmussen SA, et al. Among authors: gray ba. Am J Med Genet. 1996 Sep 6;64(4):546-50. doi: 10.1002/(SICI)1096-8628(19960906)64:4<546::AID-AJMG4>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8870920

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

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

7

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

8

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

9

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

10

Culture of cytogenetically abnormal schwann cells from benign and malignant NF1 tumors.

Wallace MR, Rasmussen SA, Lim IT, Gray BA, Zori RT, Muir D. Wallace MR, et al. Among authors: gray ba. Genes Chromosomes Cancer. 2000 Feb;27(2):117-23. Genes Chromosomes Cancer. 2000. PMID: 10612798

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