Interstitial deletion of the long arm of chromosome 1, del(1)(q21-q25) in a profoundly retarded 8-year-old girl with multiple anomalies

Author:

Schinzel A.,Schmid W.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Four further families informative for lq and the Duffy blood group;Cook;Cytogenet. Cell Genet.,1978

2. Cranio-synostosis, profound growth retardation, unusual facies, and multiple minor anomalies associated with intercalary deletion: 46, XX, del(1)(q24, q31);Crandall;Amer. J. hum. Genet.,1974

3. Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1;Garver;Clin. Genet.,1976

4. Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46, XY, del(1)(q25q32);Koivisto;Acta paediat. scand.,1976

5. Meiotic consequences of an intrachromosomal insertion of chromosome No. 1: a family pedigree;Pan;Clin. Genet.,1977

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