Works matching IS 00099163 AND DT 1997 AND VI 51 AND IP 1
Results: 19
An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousins.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 61, doi. 10.1111/j.1399-0004.1997.tb02417.x
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Symmetry of neurological signs in Pakistani patients with probable inherited spastic cerebral palsy.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 7, doi. 10.1111/j.1399-0004.1997.tb02406.x
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Spectrum of CFTR mutations in Argentine cystic fibrosis patients.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 43, doi. 10.1111/j.1399-0004.1997.tb02413.x
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Two mosaic-YY males carrying asymmetric Y chromosomes.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 65, doi. 10.1111/j.1399-0004.1997.tb02418.x
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Short Report on DNA Marker at Candidate Locus.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 76, doi. 10.1111/j.1399-0004.1997.tb02422.x
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Paracentric inversion of chromosome 9 with schizoaffective disorder.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 69, doi. 10.1111/j.1399-0004.1997.tb02419.x
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Association of angiotensin II type 1 receptor gene polymorphism with essential hypertension.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 31, doi. 10.1111/j.1399-0004.1997.tb02410.x
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Chromosome deletion 17pl 1.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 71, doi. 10.1111/j.1399-0004.1997.tb02420.x
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Genetic variation of the angiotensin-converting enzyme gene: increased frequency of the insertion allele in Koreans.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 35, doi. 10.1111/j.1399-0004.1997.tb02411.x
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Short Report on DNA Marker at Candidate Locus.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 75, doi. 10.1111/j.1399-0004.1997.tb02421.x
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- Article
Are common mutations of cystathionine β-synthase involved in the aetiology of neural tube defects?
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- Clinical Genetics, 1997, v. 51, n. 1, p. 39, doi. 10.1111/j.1399-0004.1997.tb02412.x
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'Reduction' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 1, doi. 10.1111/j.1399-0004.1997.tb02405.x
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Oculopharyngeal muscular dystrophy (OPMD)-report and genetic studies of an Australian kindred.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 52, doi. 10.1111/j.1399-0004.1997.tb02415.x
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De novo duplication of 7pter→p21.2 and deletion of 9pter→p23.5: clinical and cytogenetic diagnosis.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 56, doi. 10.1111/j.1399-0004.1997.tb02416.x
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Short Report on DNA Marker at Candidate Locus.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 78, doi. 10.1111/j.1399-0004.1997.tb02423.x
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The role of the apolipoprotein E polymorphism in the prediction of coronary artery disease age of onset.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 22, doi. 10.1111/j.1399-0004.1997.tb02408.x
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Interaction of the cholesteryl ester transfer protein I405V polymorphism with alcohol consumption in smoking and non-smoking healthy men, and the effect on plasma HDL cholesterol and apoAI concentration.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 15, doi. 10.1111/j.1399-0004.1997.tb02407.x
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Association analysis of CA repeat polymorphism of the endothelial nitric oxide synthase gene with essential hypertension in Japanese.
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- Clinical Genetics, 1997, v. 51, n. 1, p. 26, doi. 10.1111/j.1399-0004.1997.tb02409.x
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Interstitial deletion of long arm of chromosome no. 5 with growth hormone deficiency-an emerging syndrome?
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- Clinical Genetics, 1997, v. 51, n. 1, p. 48, doi. 10.1111/j.1399-0004.1997.tb02414.x
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- Article