A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility

Author:

Joseph A.,Thomas I. M.

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. A case of multiple chromosomal rearrangements with persistence of fetal hemoglobin;Nuzzo, F.; Marini, A.; Baglioni, C.; Ford, C.E.; de Carli, L.; Sereni, L.P.;Cytogenetics,1968

2. Cri-du-chat syndrome and complex chromosome rearrangement in a dizygotic twin;Taillemete, J.L.; Baheux-Morlier, G.; Cathelineau, L.; Roux, C.;Ann Genet (Paris),1973

3. A complex translocation involving chromosomes 3, 11 and 14 with an interstitial deletion, del (14) (ql3q22) in a child with congenital glaucoma and cleft lip and palate;Buchnan, P.D.; Rao, K.W.; Doerr, C.L.; Aylesworth, A.S.;Birth Defects,1978

4. Microtechnique for culturing leukocytes from whole blood;Arakaki, D.T.; Sparkes, R.S.,1963

5. A rapid banding technique for human chromosomes;Seabright, M.;Lancet,1971

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