X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivation.

Preis, W; Barbi, G; Liptay, S; Kennerknecht, I; Schwemmle, S; Pohlandt, F

Preis, W; Barbi, G; Liptay, S; Kennerknecht, I; Schwemmle, S; Pohlandt, F.

Affiliation

Preis W; Universitätskinderklinik, Ulm, Germany.

Am J Med Genet ; 61(2): 117-21, 1996 Jan 11.

Article in En | MEDLINE | ID: mdl-8669435

Subject(s)

Chromosomes, Human, Pair 16; Translocation, Genetic; Trisomy; Adult; Dosage Compensation, Genetic; Female; Humans; Infant, Newborn; Male; Metaphase; Phenotype

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Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Trisomy / Chromosomes, Human, Pair 16 Limits: Adult / Female / Humans / Male / Newborn Language: En Journal: Am J Med Genet Year: 1996 Document type: Article

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