Works matching IS 00099163 AND DT 1991 AND VI 39 AND IP 6
Results: 11
Estimates of heritability of plasma homocyst(e)ine levels in aging adult male twins.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 6, p. 425, doi. 10.1111/j.1399-0004.1991.tb03053.x
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- Article
Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 6, p. 429, doi. 10.1111/j.1399-0004.1991.tb03054.x
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- Article
Atelosteogenesis I and boomerang dysplasia: a question of nosology.
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- Clinical Genetics, 1991, v. 39, n. 6, p. 471, doi. 10.1111/j.1399-0004.1991.tb03060.x
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- Article
Malformations in a child with dup (7 pter-p15.1) and del (7 q36-qter) as a result of familial pericentric inversion.
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- Clinical Genetics, 1991, v. 39, n. 6, p. 442, doi. 10.1111/j.1399-0004.1991.tb03056.x
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- Article
A chromosome 17q de novo paracentric inversion in a patient with campomelic dysplasia; case report and etiologic hypothesis.
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- Clinical Genetics, 1991, v. 39, n. 6, p. 401, doi. 10.1111/j.1399-0004.1991.tb03050.x
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- Article
Second case report of del(4) (q25q27) and review of the literature.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 6, p. 463, doi. 10.1111/j.1399-0004.1991.tb03058.x
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- Article
A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.
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- Clinical Genetics, 1991, v. 39, n. 6, p. 434, doi. 10.1111/j.1399-0004.1991.tb03055.x
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- Article
Prenatal diagnosis of lethal osteogenesis imperfecta in twin pregnancy.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 6, p. 467, doi. 10.1111/j.1399-0004.1991.tb03059.x
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- Article
Personality in 47,XXY males during adolescence.
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- Clinical Genetics, 1991, v. 39, n. 6, p. 409, doi. 10.1111/j.1399-0004.1991.tb03051.x
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- Article
DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemia.
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- Clinical Genetics, 1991, v. 39, n. 6, p. 451, doi. 10.1111/j.1399-0004.1991.tb03057.x
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- Publication type:
- Article
Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 6, p. 419, doi. 10.1111/j.1399-0004.1991.tb03052.x
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- Publication type:
- Article