Works matching IS 00099163 AND DT 1975 AND VI 7 AND IP 3
Results: 12
A case of trisomy 8 mosaicism 47, XX, + 8/46, XX.
- Published in:
- Clinical Genetics, 1975, v. 7, n. 3, p. 232, doi. 10.1111/j.1399-0004.1975.tb00324.x
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- Article
Ring chromosome 13 syndrome.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 203, doi. 10.1111/j.1399-0004.1975.tb00320.x
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- Article
Genetics of the GPT system. Family, mother/child and association studies.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 245, doi. 10.1111/j.1399-0004.1975.tb00326.x
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- Article
Polycythemia Vera treated with.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 227, doi. 10.1111/j.1399-0004.1975.tb00323.x
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- Article
Familial occurrence of the G syndrome.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 238, doi. 10.1111/j.1399-0004.1975.tb00325.x
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- Article
The significance of 'unspecific neuropathy' in hereditary ataxias and related disorders.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 209, doi. 10.1111/j.1399-0004.1975.tb00321.x
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- Article
Familial amyotrophic lateral sclerosis with dementia: A second Canadian family.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 186, doi. 10.1111/j.1399-0004.1975.tb00317.x
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- Article
Evidence for recessive inheritance of myopia.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 197, doi. 10.1111/j.1399-0004.1975.tb00319.x
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- Article
Asymmetric septal hypertrophy in a large Amish kindred.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 255, doi. 10.1111/j.1399-0004.1975.tb00327.x
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- Article
X-linked hypoxanthine-guanine phosphoribosyltransferase deficiency without neurological disorders. A report of a family.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 181, doi. 10.1111/j.1399-0004.1975.tb00316.x
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- Article
Mental retardation and congenital malformations associated with a ring chromosome 6.
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- Clinical Genetics, 1975, v. 7, n. 3, p. 192, doi. 10.1111/j.1399-0004.1975.tb00318.x
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A computer-oriented linkage analysis scheme.
- Published in:
- Clinical Genetics, 1975, v. 7, n. 3, p. 219, doi. 10.1111/j.1399-0004.1975.tb00322.x
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- Article