Author:
Callen D. F.,Woollatt E.,Sutherland G. R.
Subject
Genetics(clinical),Genetics
Reference26 articles.
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3. Two cases of familial paracentric inversion in man associated with sex chromosome anomaly 47, XXY, inv(5)(q21, q32) and 45, X, inv(7) (q11.3q22.3);Canki;Hum. Genet.,1979
4. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing-over within the inserted segment;Cohen;Am. J. Hum. Genet.,1983
5. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis;Solar;J. Pediatr.,1974
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