Works matching IS 00099163 AND DT 1997 AND VI 52 AND IP 2
Results: 12
China's genetic services providers' attitudes towards several ethical issues: a cross-cultural survey.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 100, doi. 10.1111/j.1399-0004.1997.tb02526.x
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- Article
Developmental aspects in apple peel intestinal atresia - ocular anomalies - microcephaly syndrome.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 133, doi. 10.1111/j.1399-0004.1997.tb02532.x
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Partial trisomy 6p from a de novo translocation (6; 18) with variable mosaicism in different tissues.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 126, doi. 10.1111/j.1399-0004.1997.tb02530.x
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A DNA polymorphism at the angiotensin II type 1 receptor (AT1R) locus and myocardial infarction.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 71, doi. 10.1111/j.1399-0004.1997.tb02521.x
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Analyses of mutations in the human renal kallikrein (hKLKl) gene and their possible relevance to blood pressure regulation and risk of myocardial infarction.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 86, doi. 10.1111/j.1399-0004.1997.tb02524.x
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- Article
GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 110, doi. 10.1111/j.1399-0004.1997.tb02527.x
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- Article
Combined partial trisomy 3p/monosomy 5p resulting in sonographic abnormalities.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 96, doi. 10.1111/j.1399-0004.1997.tb02525.x
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Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 120, doi. 10.1111/j.1399-0004.1997.tb02529.x
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Apolipoproteins B and E, and angiotensin I-converting enzyme (ACE) genetic polymorphisms in Italian women with coronary artery disease (CAD) and their relationships with plasma lipid and apolipoprotein levels.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 77, doi. 10.1111/j.1399-0004.1997.tb02522.x
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A dinucleotide repeat and a Hae III polymorphism in the human nicotinic acetylcholine receptor alpha-subunit gene (CHRNA1).
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- Clinical Genetics, 1997, v. 52, n. 2, p. 130, doi. 10.1111/j.1399-0004.1997.tb02531.x
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Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 116, doi. 10.1111/j.1399-0004.1997.tb02528.x
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Association analysis of TG repeat polymorphism of the neuronal nitric oxide synthase gene with essential hypertension.
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- Clinical Genetics, 1997, v. 52, n. 2, p. 83, doi. 10.1111/j.1399-0004.1997.tb02523.x
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- Article