A partial long arm deletion of chromosome 7:46,XY,del(7)(q32).

Author:

Kousseff B G,Hsu L Y,Paciuc S,Hirschhorn K

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities;Hamerton, J.L.; Canning, N.; Ray, M.; Smith, S.;Clinical Genetics,1975

2. Correlation between euploid structural chromosome rearrangements and mental subnormality in humans;Jacobs, P.A.;Nature,1974

3. De novo occurrence of 46, XX, t (4; 13)(q31; ql4) in a mentally retarded girl;Jenkins, E.C.; Curcuru-Giordano, F.M.; Krishna, S.G.; Cantrarella, J.;Annales de Genetique,1975

4. Prenatal diagnosis of chromosome disorders;Laurence, K.M.; Gregory, P.;British Medical Bulletin; Standardization in Human Cytogenetics. Birth Defects: Original Article Series, XI,1976

5. New technique for distinguishing between human chromosomes;Sumner, A.T.; Evans, H.J.; Buckland, R.A.;Nature (New Biology),1971

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