Works matching IS 00099163 AND DT 1974 AND VI 6 AND IP 5
Results: 11
Announcement.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 422, doi. 10.1111/j.1399-0004.1974.tb02266.x
- Publication type:
- Article
Cytogenetics, hormones and behavior disability: comparison of XYY and XXY syndromes.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 370, doi. 10.1111/j.1399-0004.1974.tb02260.x
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- Publication type:
- Article
Taurodontism in X-chromosome aneuploid syndromes.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 341, doi. 10.1111/j.1399-0004.1974.tb02257.x
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- Publication type:
- Article
Trisomy for the short arm of chromosome No. 10.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 408, doi. 10.1111/j.1399-0004.1974.tb02264.x
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- Publication type:
- Article
The sex-ratio of children born to parents affected with Huntington's disease.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 345, doi. 10.1111/j.1399-0004.1974.tb02258.x
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- Publication type:
- Article
Genetics of obstetrical variables. A study from the collaborative perinatal project.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 351, doi. 10.1111/j.1399-0004.1974.tb02259.x
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- Publication type:
- Article
Are 1q+ chromosomes harmless?
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 383, doi. 10.1111/j.1399-0004.1974.tb02261.x
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- Publication type:
- Article
Hurler/Scheie genetic compound (mucopolysaccharidosis IH/IS) in Japanese brothers.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 394, doi. 10.1111/j.1399-0004.1974.tb02262.x
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- Publication type:
- Article
In vitro autoradiographic studies of DNA synthesis in human testis with spermatogenic arrest.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 401, doi. 10.1111/j.1399-0004.1974.tb02263.x
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- Publication type:
- Article
Adult-onset hereditary cerebellar ataxia and neurosensory deafness.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 416, doi. 10.1111/j.1399-0004.1974.tb02265.x
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- Publication type:
- Article
A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation.
- Published in:
- Clinical Genetics, 1974, v. 6, n. 5, p. 335, doi. 10.1111/j.1399-0004.1974.tb02256.x
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- Publication type:
- Article