Event-related potentials (ERPs) and intelligence in neonatally identified 47, XXY males.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 150, doi. 10.1111/j.1399-0004.1995.tb03948.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1995 AND VI 47 AND IP 3
Results: 13
1
2
Clinical and molecular genetic findings in five patients with Miller-Dieker syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 161, doi. 10.1111/j.1399-0004.1995.tb03951.x
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- Publication type:
- Article
3
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 125, doi. 10.1111/j.1399-0004.1995.tb03944.x
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- Publication type:
- Article
4
Dinucleotide repeat polymorphism at the human CD59 locus.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 165, doi. 10.1111/j.1399-0004.1995.tb03952.x
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- Publication type:
- Article
5
Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 118, doi. 10.1111/j.1399-0004.1995.tb03942.x
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- Publication type:
- Article
6
Cytogenetic analysis of 23 Japanese patients with amyotrophic lateral sclerosis.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 158, doi. 10.1111/j.1399-0004.1995.tb03950.x
- By:
- Publication type:
- Article
7
Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 113, doi. 10.1111/j.1399-0004.1995.tb03941.x
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- Publication type:
- Article
8
A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 139, doi. 10.1111/j.1399-0004.1995.tb03946.x
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- Publication type:
- Article
9
Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 122, doi. 10.1111/j.1399-0004.1995.tb03943.x
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- Publication type:
- Article
10
Familial benign setting-sun phenomenon in healthy newborns.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 167, doi. 10.1111/j.1399-0004.1995.tb03953.x
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- Publication type:
- Article
11
Exclusion mapping of the benign hereditary chorea gene from the Huntington's disease locus: report of a family.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 133, doi. 10.1111/j.1399-0004.1995.tb03945.x
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- Publication type:
- Article
12
Quantitation of fibrillin immunofluorescence in fibroblast cultures in the Marfan syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 144, doi. 10.1111/j.1399-0004.1995.tb03947.x
- By:
- Publication type:
- Article
13
Confidentiality in counseling for X-linked conditions.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 3, p. 155, doi. 10.1111/j.1399-0004.1995.tb03949.x
- By:
- Publication type:
- Article