Cassidy SB - Search Results

1

Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15.

Gunay-Aygun M, Heeger S, Schwartz S, Cassidy SB. Gunay-Aygun M, et al. Among authors: cassidy sb. Am J Med Genet. 1997 Jul 11;71(1):106-10. Am J Med Genet. 1997. PMID: 9215778

2

Prader-Willi syndrome.

Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Cassidy SB, et al. Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26. Genet Med. 2012. PMID: 22237428 Free article. Review.

3

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.

Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwartz S. Cassidy SB, et al. Am J Med Genet. 1997 Feb 11;68(4):433-40. Am J Med Genet. 1997. PMID: 9021017

4

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.

Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD. Saitoh S, et al. Among authors: cassidy sb. Am J Med Genet. 1997 Jan 20;68(2):195-206. Am J Med Genet. 1997. PMID: 9028458

5

Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.

Conroy JM, Grebe TA, Becker LA, Tsuchiya K, Nicholls RD, Buiting K, Horsthemke B, Cassidy SB, Schwartz S. Conroy JM, et al. Among authors: cassidy sb. Am J Hum Genet. 1997 Aug;61(2):388-94. doi: 10.1086/514852. Am J Hum Genet. 1997. PMID: 9311744 Free PMC article.

6

Prader-Willi and other syndromes associated with obesity and mental retardation.

Gunay-Aygun M, Cassidy SB, Nicholls RD. Gunay-Aygun M, et al. Among authors: cassidy sb. Behav Genet. 1997 Jul;27(4):307-24. doi: 10.1023/a:1025683829856. Behav Genet. 1997. PMID: 9519559 Review.

7

Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.

Cassidy SB, Schwartz S. Cassidy SB, et al. Medicine (Baltimore). 1998 Mar;77(2):140-51. doi: 10.1097/00005792-199803000-00005. Medicine (Baltimore). 1998. PMID: 9556704 Free article. Review.

8

Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.

Amos-Landgraf JM, Ji Y, Gottlieb W, Depinet T, Wandstrat AE, Cassidy SB, Driscoll DJ, Rogan PK, Schwartz S, Nicholls RD. Amos-Landgraf JM, et al. Among authors: cassidy sb. Am J Hum Genet. 1999 Aug;65(2):370-86. doi: 10.1086/302510. Am J Hum Genet. 1999. PMID: 10417280 Free PMC article.

9

Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl.

Kumar A, Cassidy SB, Romero L, Schwartz S. Kumar A, et al. Among authors: cassidy sb. Am J Med Genet. 1999 Sep 17;86(3):227-31. doi: 10.1002/(sici)1096-8628(19990917)86:3<227::aid-ajmg6>3.0.co;2-3. Am J Med Genet. 1999. PMID: 10482870

10

Molecular refinement of karyotype: beyond the cytogenetic band.

Sirko-Osadsa DA, Cassidy SB, Depinet TW, Robin NH, Limwongse C, Schwartz S. Sirko-Osadsa DA, et al. Among authors: cassidy sb. Genet Med. 1999 Sep-Oct;1(6):254-61. doi: 10.1097/00125817-199909000-00003. Genet Med. 1999. PMID: 11258626 Free article.

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