Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 5, p. 365, doi. 10.1111/j.1399-0004.1983.tb00087.x
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- Publication type:
- Article
Works matching IS 00099163 AND DT 1983 AND VI 24 AND IP 5
Results: 6
1
2
Partial trisomy 16q in two boys resulting from a maternal translocation, t(15;16) (p12;q11).
- Published in:
- Clinical Genetics, 1983, v. 24, n. 5, p. 375, doi. 10.1111/j.1399-0004.1983.tb00088.x
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- Publication type:
- Article
3
Cystic hygroma and hydrops fetalis in a fetus with trisomy 13.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 5, p. 389, doi. 10.1111/j.1399-0004.1983.tb00091.x
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- Publication type:
- Article
4
A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 5, p. 380, doi. 10.1111/j.1399-0004.1983.tb00089.x
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- Publication type:
- Article
5
45 XO/49 XYYYY Mosaicism in a male with stigmata of Turner's syndrome.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 5, p. 384, doi. 10.1111/j.1399-0004.1983.tb00090.x
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- Publication type:
- Article
6
Two cases of prenatal diagnosis of a satellited Yq chromosome.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 5, p. 359, doi. 10.1111/j.1399-0004.1983.tb00086.x
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- Publication type:
- Article