Violence sells von Soltan, H C

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Genetic testing and eugenics von Soltan, H C

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Unravelling genes: history, health care and the techno-industrial imperative von Soltan, H C

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Echinocytes in families with Duchenne muscular dystrophy von Soltan, H C

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Additional evidence for fragile X activity in heterozygous carriers von UCHIDA, I. A, FREEMAN, V. C. P, JAMRO, H, PARTINGTON, M. W, SOLTAN, H. C

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Maternal serum alpha-fetoprotein screening: report of a Canadian pilot project von Doran, T A, Valentine, G H, Wong, P Y, Wielgosz, G, Benzie, R J, Soltan, H C, Jenner, M R, Morland, P A, Montgomery, R J, Allen, L C

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PKU screening von Soltan, H C

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The extent of genetic disease in hospital populations von Soltan, H C, Craven, J L

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Familial occurrence of malformations possibly attributable to vascular abnormalities von Soltan, Hubert C., Holmes, Lewis B.

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Atypical severe muscular dystrophy in a male: genetic implications for female relatives von Soltan, H C, Pyatt, Z, Hinton, G G

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Dermatoglyphics in translocation Down's syndrome von Soltan, H C, Clearwater, K

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Dermatoglyphics in Klinefelter's Syndrome (47, XXY) von Cushman, C. J., Soltan, H. C.

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Duchen: An interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in duchenne muscular dystrophy von Andrews, David F., Brasher, Penelope M. A., Manchester, Kathryn E., Percy, Maire E., Rusk, Ann C. M., Soltan, Hubert C., Trueman, David W., Reynolds, James F.

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Male pseudohermaphroditism and pure gonadal dysgenesis in sisters von Barr, Murray L., Carr, David H., Plunkett, Earl R., Soltan, Hubert C., Wiens, Ruth G.

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Genetic characteristics of families of XO and XXY patients, including evidence of source of X chromosomes in 7 aneuploid patients von Soltan, H C

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A 13-15/21 translocation chromosome in carrier father and mongol son von SERGOVICH, F R, SOLTAN, H C, CARR, D H

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Counselling families on genetic problems von Soltan, H C

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THE XXYY VARIANT OF KLINEFELTER'S SYNDROME von BARR, M L, CARR, D H, SOLTAN, H C, WIENS, R G, PLUNKETT, E R

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Thoughts on learning and teaching in the first two years of the medical curriculum von Soltan, H C

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DERMATOGLYPHICS ASSOCIATED WITH THE XXYH CHROMOSOME COMPLEMENT von UCHIDA, I A, MILLER, J R, SOLTAN, H C

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