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Article

Hypogammaglobulinemia and Silver-Russell phenotype associated with partial trisomy 7q and partial monosomy 21q.

American journal of medical genetics. Part A - 1 Feb 2009

Artac Hasibe, Reisli Ismail, Yildirim Mahmut Selman, Bagci Gulseren, Luleci Guven, Hosgor Orhan, Karaaslan Sevim

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Identifiers

PMID: 19161136
DOI: 10.1002/ajmg.a.32617

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Hypogammaglobulinemia and Silver-Russell phenotype associated with partial trisomy 7q and partial monosomy 21q.PMID 19161136Read ↗

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Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?Semantic proximity Read ↗

Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver–Russell syndromeSemantic proximity Read ↗

Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome.Semantic proximity Read ↗

Genetics of Silver-Russell syndrome.Semantic proximity Read ↗

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Mosaic upd(7)mat in a patient with Silver-Russell syndrome.Semantic proximity Read ↗

Silver-Russell syndrome and exclusion of uniparental disomy.Semantic proximity Read ↗

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