Works matching IS 00099163 AND DT 1991 AND VI 40 AND IP 6
Results: 13
Cohen syndrome: fertility in a female patient.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 461, doi. 10.1111/j.1399-0004.1991.tb03118.x
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- Article
Chromosome aberrations in Sotos syndrome.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 472, doi. 10.1111/j.1399-0004.1991.tb03122.x
- Publication type:
- Article
Diagnostic reliability of the cytogenetic centromere heteromorphism in the human X chromosome.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 465, doi. 10.1111/j.1399-0004.1991.tb03119.x
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- Article
Robertsonian translocations in Prader-Willi syndrome.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 471, doi. 10.1111/j.1399-0004.1991.tb03121.x
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- Article
Genetic mapping of loci for X-linked retinitis pigmentosa.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 435, doi. 10.1111/j.1399-0004.1991.tb03115.x
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- Article
De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 417, doi. 10.1111/j.1399-0004.1991.tb03112.x
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- Article
Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 430, doi. 10.1111/j.1399-0004.1991.tb03114.x
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- Article
Tests of performance of four semiautomatic metaphase-finding and karyotyping systems.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 441, doi. 10.1111/j.1399-0004.1991.tb03116.x
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- Publication type:
- Article
Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 452, doi. 10.1111/j.1399-0004.1991.tb03117.x
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- Publication type:
- Article
Simultaneous expression of the rare and common fragile sites on the X chromosome.
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- Clinical Genetics, 1991, v. 40, n. 6, p. 423, doi. 10.1111/j.1399-0004.1991.tb03113.x
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- Article
Erratum.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 474, doi. 10.1111/j.1399-0004.1991.tb03124.x
- Publication type:
- Article
An autosomal recessive form of benign familial neonatal seizures.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 467, doi. 10.1111/j.1399-0004.1991.tb03120.x
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- Publication type:
- Article
Announcement.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 6, p. 473, doi. 10.1111/j.1399-0004.1991.tb03123.x
- Publication type:
- Article