9710025 8744026 9237260 27594721 8030667 9415690 10417280 7977469 20891031 8571960 9028458 8160752 8882776 7604853 9580159 10740202 8388169 9288101 8111367 8540683 7611294 9188662 7747771 7625450 1584261 23776360 9102354 8669451 9741464 7573182 89299 - Search Results

Year	Number of Results
1992	1
1993	2
1994	3
1995	6
1996	7
1997	5
1998	3
1999	1
2000	1
2010	2
2022	0

1

Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation.

Guerrini R, Dobyns WB. Guerrini R, et al. Neurology. 1998 Aug;51(2):499-503. doi: 10.1212/wnl.51.2.499. Neurology. 1998. PMID: 9710025

2

Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effect.

Mignon C, Malzac P, Moncla A, Depetris D, Roeckel N, Croquette MF, Mattei MG. Mignon C, et al. Eur J Hum Genet. 1996;4(2):88-100. doi: 10.1159/000472176. Eur J Hum Genet. 1996. PMID: 8744026

3

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.

Glenn CC, Driscoll DJ, Yang TP, Nicholls RD. Glenn CC, et al. Mol Hum Reprod. 1997 Apr;3(4):321-32. doi: 10.1093/molehr/3.4.321. Mol Hum Reprod. 1997. PMID: 9237260 Review.

4

Prader-Willi Syndrome: Genetics and Behavior.

Thompson T, Butler MG, MacLean WE Jr, Joseph B. Thompson T, et al. Peabody J Educ. 1996;71(4):187-212. doi: 10.1080/01619569609595137. Peabody J Educ. 1996. PMID: 27594721 Free PMC article.

5

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?

Bottani A, Robinson WP, DeLozier-Blanchet CD, Engel E, Morris MA, Schmitt B, Thun-Hohenstein L, Schinzel A. Bottani A, et al. Am J Med Genet. 1994 May 15;51(1):35-40. doi: 10.1002/ajmg.1320510109. Am J Med Genet. 1994. PMID: 8030667

6

Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR method.

Kosaki K, McGinniss MJ, Veraksa AN, McGinnis WJ, Jones KL. Kosaki K, et al. Am J Med Genet. 1997 Dec 19;73(3):308-13. Am J Med Genet. 1997. PMID: 9415690

7

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. Am J Hum Genet. 1999 Aug;65(2):370-86. doi: 10.1086/302510. Am J Hum Genet. 1999. PMID: 10417280 Free PMC article.

8

Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.

Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA. Delach JA, et al. Am J Med Genet. 1994 Aug 1;52(1):85-91. doi: 10.1002/ajmg.1320520117. Am J Med Genet. 1994. PMID: 7977469

9

Diagnosis of cryptic chromosomal syndromes by fluorescence in situ hybridization (FISH).

Kashork CD, Theisen A, Shaffer LG. Kashork CD, et al. Curr Protoc Hum Genet. 2010 Oct;Chapter 8:Unit 8.10.1-20. doi: 10.1002/0471142905.hg0810s67. Curr Protoc Hum Genet. 2010. PMID: 20891031

10

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Glenn CC, Saitoh S, Jong MT, Filbrandt MM, Surti U, Driscoll DJ, Nicholls RD. Glenn CC, et al. Am J Hum Genet. 1996 Feb;58(2):335-46. Am J Hum Genet. 1996. PMID: 8571960 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results