Cassidy SB - Search Results

1

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

2

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

Cassidy SB, Lai LW, Erickson RP, Magnuson L, Thomas E, Gendron R, Herrmann J. Cassidy SB, et al. Am J Hum Genet. 1992 Oct;51(4):701-8. Am J Hum Genet. 1992. PMID: 1357962 Free PMC article.

3

Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13.

Orstavik KH, Tangsrud SE, Kiil R, Hansteen IL, Steen-Johnsen J, Cassidy SB, Martony A, Anvret M, Tommerup N, Bröndum-Nielsen K. Orstavik KH, et al. Among authors: cassidy sb. Am J Med Genet. 1992 Nov 1;44(4):534-8. doi: 10.1002/ajmg.1320440431. Am J Med Genet. 1992. PMID: 1442901

4

7p deletion syndrome: an adult with mild manifestations.

Grebe TA, Stevens MA, Byrne-Essif K, Cassidy SB. Grebe TA, et al. Among authors: cassidy sb. Am J Med Genet. 1992 Sep 1;44(1):18-23. doi: 10.1002/ajmg.1320440106. Am J Med Genet. 1992. PMID: 1519644

5

Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.

Aughton DJ, Cassidy SB, Whiteman DA, Delach JA, Guttmacher AE. Aughton DJ, et al. Among authors: cassidy sb. Am J Med Genet. 1991 Sep 15;40(4):440-3. doi: 10.1002/ajmg.1320400412. Am J Med Genet. 1991. PMID: 1746608

6

Hand and foot length in Prader-Willi syndrome.

Hudgins L, Cassidy SB. Hudgins L, et al. Among authors: cassidy sb. Am J Med Genet. 1991 Oct 1;41(1):5-9. doi: 10.1002/ajmg.1320410103. Am J Med Genet. 1991. PMID: 1951464

7

Physical features of Prader-Willi syndrome in neonates.

Aughton DJ, Cassidy SB. Aughton DJ, et al. Among authors: cassidy sb. Am J Dis Child. 1990 Nov;144(11):1251-4. doi: 10.1001/archpedi.1990.02150350083032. Am J Dis Child. 1990. PMID: 2239867

8

Cephalometric analysis of the Prader-Willi syndrome.

Schaedel R, Poole AE, Cassidy SB. Schaedel R, et al. Among authors: cassidy sb. Am J Med Genet. 1990 Aug;36(4):484-7. doi: 10.1002/ajmg.1320360423. Am J Med Genet. 1990. PMID: 2389807

9

Prader-Willi syndrome.

Cassidy SB, Ledbetter DH. Cassidy SB, et al. Neurol Clin. 1989 Feb;7(1):37-54. Neurol Clin. 1989. PMID: 2646521 Review.

10

Occupational hydrocarbon exposure among fathers of Prader-Willi syndrome patients with and without deletions of 15q.

Cassidy SB, Gainey AJ, Butler MG. Cassidy SB, et al. Am J Hum Genet. 1989 Jun;44(6):806-10. Am J Hum Genet. 1989. PMID: 2729276 Free PMC article.

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