Report of the first international works... [Cytogenet Cell Genet. 1992] - PubMed

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Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15. [Hum Mol Genet. 1992]
Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.
Mutirangura A, Kuwano A, Ledbetter SA, Chinault AC, Ledbetter DH. Hum Mol Genet. 1992 May; 1(2):139.
Dinucleotide repeat polymorphism at the GABAA receptor beta 3 (GABRB3) locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15. [Hum Mol Genet. 1992]
Dinucleotide repeat polymorphism at the GABAA receptor beta 3 (GABRB3) locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.
Mutirangura A, Ledbetter SA, Kuwano A, Chinault AC, Ledbetter DH. Hum Mol Genet. 1992 Apr; 1(1):67.
PCR-based strategies for the diagnosis of Prader-Willi/Angelman syndromes. [Methods Mol Biol. 2003]
PCR-based strategies for the diagnosis of Prader-Willi/Angelman syndromes.
Velinov M, Jenkins EC. Methods Mol Biol. 2003; 217:209-16.
Review Recombination model for generation of a submicroscopic deletion in familial Angelman syndrome. [Hum Mol Genet. 1994]
Review Recombination model for generation of a submicroscopic deletion in familial Angelman syndrome.
Nicholls RD. Hum Mol Genet. 1994 Jan; 3(1):9-11.
Review Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview. [Am J Med Genet. 1993]
Review Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.
Knoll JH, Wagstaff J, Lalande M. Am J Med Genet. 1993 Apr 1; 46(1):2-6.

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Cited by 3 PubMed Central articles

Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier. [Mol Cytogenet. 2009]
Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier.
Mantzouratou A, Mania A, Apergi M, Laver S, Serhal P, Delhanty J. Mol Cytogenet. 2009 Jan 23; 2:3. Epub 2009 Jan 23.
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families. [J Med Genet. 1997]
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.
Gilbert HL, Buxton JL, Chan CT, McKay T, Cottrell S, Ramsden S, Winter RM, Pembrey ME, Malcolm S. J Med Genet. 1997 Aug; 34(8):651-5.
Molecular mechanisms in Angelman syndrome: a survey of 93 patients. [J Med Genet. 1993]
Molecular mechanisms in Angelman syndrome: a survey of 93 patients.
Chan CT, Clayton-Smith J, Cheng XJ, Buxton J, Webb T, Pembrey ME, Malcolm S. J Med Genet. 1993 Nov; 30(11):895-902.

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Report of the first international workshop on human chromosome 15 mapping.
Report of the first international workshop on human chromosome 15 mapping.
Cytogenet Cell Genet. 1992 ;61(3):162-6.

PubMed
[Mosaicism-trisomy in fathers of two children with Down's syndrome].
[Mosaicism-trisomy in fathers of two children with Down's syndrome].
Acta Paediatr Acad Sci Hung. 1976 ;17(3):177-81.

PubMed
MOSAIC TRISOMY IN PHENOTYPICALLY NORMAL MOTHER OF MONGOL.
MOSAIC TRISOMY IN PHENOTYPICALLY NORMAL MOTHER OF MONGOL.
Lancet. 1964 Mar 7 ;1(7332):526-7.

PubMed
Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.
Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.
Am J Hum Genet. 1992 Jan ;50(1):15-28.

PubMed
The distal triradius t on the hands of parents and sibs of mongol imbeciles.
The distal triradius t on the hands of parents and sibs of mongol imbeciles.
Ann Hum Genet. 1954 Jul ;19(1):10-38.

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