Works matching IS 00099163 AND DT 1977 AND VI 12 AND IP 2
Results: 12
An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 65, doi. 10.1111/j.1399-0004.1977.tb00903.x
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- Article
Wolf-Hirschhorn syndrome and balanced (4;10) translocation in the father.
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- Clinical Genetics, 1977, v. 12, n. 2, p. 101, doi. 10.1111/j.1399-0004.1977.tb00909.x
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- Article
Male with 45, X karyotype.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 97, doi. 10.1111/j.1399-0004.1977.tb00908.x
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- Article
A t(5p-;21q+) translocation in a family with Down syndrome.
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- Clinical Genetics, 1977, v. 12, n. 2, p. 111, doi. 10.1111/j.1399-0004.1977.tb00911.x
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- Article
Distribution patterns of satellite associations in human lymphocytes relative to age and sex.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 104, doi. 10.1111/j.1399-0004.1977.tb00910.x
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- Article
Linkage analysis with misclassification at one locus.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 119, doi. 10.1111/j.1399-0004.1977.tb00913.x
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- Article
Bloom's syndrome in two Dutch families.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 85, doi. 10.1111/j.1399-0004.1977.tb00907.x
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- Article
Insertional translocation into the X chromosome of a 46, XY male.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 114, doi. 10.1111/j.1399-0004.1977.tb00912.x
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- Article
A problem for genetic counselling - split hand deformity.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 125, doi. 10.1111/j.1399-0004.1977.tb00914.x
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- Article
The deletion 9p syndrome. A 61-year-old man with deletion of short arm 9.
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- Clinical Genetics, 1977, v. 12, n. 2, p. 80, doi. 10.1111/j.1399-0004.1977.tb00906.x
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- Article
Genetic variance of erythrocyte parameters in adult male twins.
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- Clinical Genetics, 1977, v. 12, n. 2, p. 73, doi. 10.1111/j.1399-0004.1977.tb00904.x
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- Article
Alpha-I-antitrypsin (Pi) phenotypes in Lyon, France: departure from Hardy-Weinberg equilibrium.
- Published in:
- Clinical Genetics, 1977, v. 12, n. 2, p. 77, doi. 10.1111/j.1399-0004.1977.tb00905.x
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- Article