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Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-.
Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet].
Show details- Kirchhoff M, Rose H, Lundsteen C.: High resolution comparative genomic hybridisation in clinical cytogenetics. J. Med. Genet. 38:740-744, 2001. [PMC free article: PMC1734756] [PubMed: 11694545]Case No. 21=46,XX,r(13).rev ish dim(13p11.2q22).The patient was dysmorphic with malformations.Aberration: RI,TDChromosomal Aneuploidy: 13q-
- Slater H, Shaw J H, Bankier A, Forrest S M, Dawson G.: UPD 13: no indication of maternal or paternal imprinting of genes on chromosome 13. J. Med. Genet. 32:493, 1995. [PMC free article: PMC1050497] [PubMed: 7666408]
Slater H, Shaw J H, Dawson G, Bankier A, Forrest S M: Maternal uniparental disomy of chromosome 13 in a phenotypically normal child. J. Med. Genet. 31:644-646, 1994. [PMC free article: PMC1050029] [PubMed: 7815424]Proband:45,XY,der t(13;13)(p11.2;p11.2)mat.&"45,XX,-13,-13,+t(13;13)(p11.2;p11.2)."Aberration: TR,UPDIndex Terms: Uniparental disomy (UPD)Variable band - Takahashi Y, Narahara K, Kimoto H: Determination of Esterase D (EsD) genotype in cases with trisomy 13. Jpn. J. Hum. Genet. 31:273-287, 1986. [PubMed: 3560513]Three cases of partial trisomy (1, 2, and 3) 13q(q1411 to qter) and two cases of full trisomy (4 and 5).Chromosomal polymorphisms and isozyme patterns were useful in determining the parental origin of nondisjunction.&Father: 46,XY,inv(13)(p112q1411).&46,XY,rec(13),dup q,inv(13)(p11.2q14.11)pat.Aberration: Inversion pericentricMIM#: 133280Chromosomal Aneuploidy: 13q+Index Terms: Patau syndrome (trisomy 13)Variable band
- 13p112 - Chromosomal Variation in Man13p112 - Chromosomal Variation in Man
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