Wagstaff J - Search Results

1

Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation.

Williams CA, Angelman H, Clayton-Smith J, Driscoll DJ, Hendrickson JE, Knoll JH, Magenis RE, Schinzel A, Wagstaff J, Whidden EM, et al. Williams CA, et al. Among authors: wagstaff j. Am J Med Genet. 1995 Mar 27;56(2):237-8. doi: 10.1002/ajmg.1320560224. Am J Med Genet. 1995. PMID: 7625452 No abstract available.

2

Angelman syndrome 2005: updated consensus for diagnostic criteria.

Williams CA, Beaudet AL, Clayton-Smith J, Knoll JH, Kyllerman M, Laan LA, Magenis RE, Moncla A, Schinzel AA, Summers JA, Wagstaff J. Williams CA, et al. Among authors: wagstaff j. Am J Med Genet A. 2006 Mar 1;140(5):413-8. doi: 10.1002/ajmg.a.31074. Am J Med Genet A. 2006. PMID: 16470747

3

Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.

Knoll JH, Wagstaff J, Lalande M. Knoll JH, et al. Among authors: wagstaff j. Am J Med Genet. 1993 Apr 1;46(1):2-6. doi: 10.1002/ajmg.1320460103. Am J Med Genet. 1993. PMID: 8388170 Review.

4

Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.

Knoll JH, Asamoah A, Pletcher BA, Wagstaff J. Knoll JH, et al. Among authors: wagstaff j. Am J Med Genet. 1995 Jan 16;55(2):221-4. doi: 10.1002/ajmg.1320550214. Am J Med Genet. 1995. PMID: 7717422 Review.

5

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.

Robinson WP, Wagstaff J, Bernasconi F, Baccichetti C, Artifoni L, Franzoni E, Suslak L, Shih LY, Aviv H, Schinzel AA. Robinson WP, et al. Among authors: wagstaff j. J Med Genet. 1993 Sep;30(9):756-60. doi: 10.1136/jmg.30.9.756. J Med Genet. 1993. PMID: 8411071 Free PMC article.

6

Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

Greger V, Knoll JH, Wagstaff J, Woolf E, Lieske P, Glatt H, Benn PA, Rosengren SS, Lalande M. Greger V, et al. Among authors: wagstaff j. Am J Hum Genet. 1997 Mar;60(3):574-80. Am J Hum Genet. 1997. PMID: 9042916 Free PMC article.

7

Complex familial rearrangement of chromosome 9p24.3 detected by FISH.

Repetto GM, Wagstaff J, Korf BR, Knoll JH. Repetto GM, et al. Among authors: wagstaff j. Am J Med Genet. 1998 Apr 1;76(4):306-9. Am J Med Genet. 1998. PMID: 9545094

8

Genetic counseling in Angelman syndrome: gonadal mosaicism.

Stalker HJ, Williams CA, Wagstaff J. Stalker HJ, et al. Among authors: wagstaff j. Am J Med Genet. 1998 Aug 6;78(5):482. Am J Med Genet. 1998. PMID: 9714017 No abstract available.

9

Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression.

Wagstaff J, Knoll JH, Glatt KA, Shugart YY, Sommer A, Lalande M. Wagstaff J, et al. Nat Genet. 1992 Jul;1(4):291-4. doi: 10.1038/ng0792-291. Nat Genet. 1992. PMID: 1338769

10

FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions.

Knoll JH, Sinnett D, Wagstaff J, Glatt K, Wilcox AS, Whiting PM, Wingrove P, Sikela JM, Lalande M. Knoll JH, et al. Among authors: wagstaff j. Hum Mol Genet. 1993 Feb;2(2):183-9. doi: 10.1093/hmg/2.2.183. Hum Mol Genet. 1993. PMID: 8388764

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