Zori RT - Search Results

1

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: zori rt. Genes Chromosomes Cancer. 2000 Feb;27(2):117-23. Genes Chromosomes Cancer. 2000. PMID: 10612798

2

Angelman syndrome: clinical profile.

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

3

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: zori rt. Am J Med Genet. 1990 Mar;35(3):350-3. doi: 10.1002/ajmg.1320350308. Am J Med Genet. 1990. PMID: 2309781

4

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. Am J Hum Genet. 1995 Jun;56(6):1411-6. Am J Hum Genet. 1995. PMID: 7762564 Free PMC article.

5

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: zori rt. Am J Med Genet. 1993 Apr 1;46(1):7-11. doi: 10.1002/ajmg.1320460104. Am J Med Genet. 1993. PMID: 8098583

6

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: zori rt. Am J Med Genet. 1994 May 1;50(4):368-74. doi: 10.1002/ajmg.1320500414. Am J Med Genet. 1994. PMID: 8209918

7

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. Am J Med Genet. 1993 Sep 15;47(4):504-11. doi: 10.1002/ajmg.1320470414. Am J Med Genet. 1993. PMID: 8256814

8

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. Am J Med Genet. 1993 Jun 1;46(4):379-83. doi: 10.1002/ajmg.1320460407. Am J Med Genet. 1993. PMID: 8357008

9

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: zori rt. 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

10

NF1 mutation analysis using a combined heteroduplex/SSCP approach.

Abernathy CR, Rasmussen SA, Stalker HJ, Zori R, Driscoll DJ, Williams CA, Kousseff BG, Wallace MR. Abernathy CR, et al. Hum Mutat. 1997;9(6):548-54. doi: 10.1002/(SICI)1098-1004(1997)9:6<548::AID-HUMU8>3.0.CO;2-Y. Hum Mutat. 1997. PMID: 9195229

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