Wagstaff J - Search Results

1

17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one.

Asamoah A, North K, Doran S, Wagstaff J, Ogle R, Collins FS, Korf BR. Asamoah A, et al. Among authors: wagstaff j. Am J Med Genet. 1995 Aug 14;60(4):312-6. doi: 10.1002/ajmg.1320600410. Am J Med Genet. 1995. PMID: 7485267

2

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.

3

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

4

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.

5

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.

6

High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients.

Sinnett D, Wagstaff J, Glatt K, Woolf E, Kirkness EJ, Lalande M. Sinnett D, et al. Among authors: wagstaff j. Am J Hum Genet. 1993 Jun;52(6):1216-29. Am J Hum Genet. 1993. PMID: 8389098 Free PMC article.

7

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.

8

A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.

Wagstaff J, Hemann M. Wagstaff J, et al. Am J Hum Genet. 1995 Jan;56(1):302-9. Am J Hum Genet. 1995. PMID: 7825591 Free PMC article.

9

Molecular and clinical study of 61 Angelman syndrome patients.

Saitoh S, Harada N, Jinno Y, Hashimoto K, Imaizumi K, Kuroki Y, Fukushima Y, Sugimoto T, Renedo M, Wagstaff J, et al. Saitoh S, et al. Among authors: wagstaff j. Am J Med Genet. 1994 Aug 15;52(2):158-63. doi: 10.1002/ajmg.1320520207. Am J Med Genet. 1994. PMID: 7802001 Review.

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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