Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.

No abstract is available for this paper.

• Publication year

  1997

• Venue

  American Journal of Human Genetics

• Publication date

  1997-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1086/514852PMID 9311744PMCID PMC1715912
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1997cited by this paper
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  1996cited by this paper
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  1996cited by this paper
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  1996cited by this paper
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  1996cited by this paper
• Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.

  1996cited by this paper
• Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

  1996cited by this paper
• Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient.

  1996cited by this paper
• Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.

  1995cited by this paper
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

  1995cited by this paper
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  1995cited by this paper
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  1995cited by this paper
• Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.

  1994cited by this paper
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  1994cited by this paper
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  1994cited by this paper
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  1994cited by this paper
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  1993cited by this paper
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  1993cited by this paper
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  1993cited by this paper
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