Rogan PK - Search Results

1

Relaxation of imprinting in Prader-Willi syndrome.

Rogan PK, Seip JR, White LM, Wenger SL, Steele MW, Sperling MA, Menon R, Knoll JH. Rogan PK, et al. Hum Genet. 1998 Dec;103(6):694-701. doi: 10.1007/s004390050893. Hum Genet. 1998. PMID: 9921905

2

A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region.

Gabriel J, Gottlieb W, Garcia A, Rogan PK, Saitoh S, Nicholls RD. Gabriel J, et al. Among authors: rogan pk. Hum Mol Genet. 1994 Oct;3(10):1912. doi: 10.1093/hmg/3.10.1912. Hum Mol Genet. 1994. PMID: 7849727 No abstract available.

3

Bloom syndrome and maternal uniparental disomy for chromosome 15.

Woodage T, Prasad M, Dixon JW, Selby RE, Romain DR, Columbano-Green LM, Graham D, Rogan PK, Seip JR, Smith A, et al. Woodage T, et al. Among authors: rogan pk. Am J Hum Genet. 1994 Jul;55(1):74-80. Am J Hum Genet. 1994. PMID: 7912890 Free PMC article.

4

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns.

Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Zaragoza MV, et al. Hum Genet. 1994 Oct;94(4):411-7. doi: 10.1007/BF00201603. Hum Genet. 1994. PMID: 7927339

5

Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia.

Rogan PK, Close P, Blouin JL, Seip JR, Gannutz L, Ladda RL, Antonarakis SE. Rogan PK, et al. Am J Med Genet. 1995 Nov 6;59(2):174-81. doi: 10.1002/ajmg.1320590212. Am J Med Genet. 1995. PMID: 8588582

6

Association of a mosaic chromosomal 22q11 deletion with hypoplastic left heart syndrome.

Consevage MW, Seip JR, Belchis DA, Davis AT, Baylen BG, Rogan PK. Consevage MW, et al. Among authors: rogan pk. Am J Cardiol. 1996 May 1;77(11):1023-5. doi: 10.1016/s0002-9149(97)89165-5. Am J Cardiol. 1996. PMID: 8644631

7

Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.

White LM, Rogan PK, Nicholls RD, Wu BL, Korf B, Knoll JH. White LM, et al. Among authors: rogan pk. Am J Hum Genet. 1996 Aug;59(2):423-30. Am J Hum Genet. 1996. PMID: 8755930 Free PMC article.

8

Distinct 15q genotypes in Russell-Silver and ring 15 syndromes.

Rogan PK, Seip JR, Driscoll DJ, Papenhausen PR, Johnson VP, Raskin S, Woodward AL, Butler MG. Rogan PK, et al. Am J Med Genet. 1996 Mar 1;62(1):10-5. doi: 10.1002/(SICI)1096-8628(19960301)62:1<10::AID-AJMG3>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8779316 Free PMC article.

9

Relationship of sleep abnormalities to patient genotypes in Prader-Willi syndrome.

Vgontzas AN, Kales A, Seip J, Mascari MJ, Bixler EO, Myers DC, Vela-Bueno AV, Rogan PK. Vgontzas AN, et al. Among authors: rogan pk. Am J Med Genet. 1996 Sep 20;67(5):478-82. doi: 10.1002/(SICI)1096-8628(19960920)67:5<478::AID-AJMG7>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8886165

10

Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridization.

Mowery-Rushton PA, Hanchett JM, Zipf WB, Rogan PK, Surti U. Mowery-Rushton PA, et al. Among authors: rogan pk. Am J Med Genet. 1996 Dec 30;66(4):403-12. doi: 10.1002/(SICI)1096-8628(19961230)66:4<403::AID-AJMG4>3.0.CO;2-L. Am J Med Genet. 1996. Retraction in: Am J Med Genet. 2000 Jan 17;90(2):177. PMID: 8989457 Retracted.

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