Works matching IS 00099163 AND DT 1995 AND VI 47 AND IP 1
Results: 11
Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 42, doi. 10.1111/j.1399-0004.1995.tb03920.x
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Risk estimates for developing motor neurone disease in first-degree relatives.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 13, doi. 10.1111/j.1399-0004.1995.tb03914.x
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Antley-Bixler syndrome and esophageal atresia in a patient with trisomy 21.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 53, doi. 10.1111/j.1399-0004.1995.tb03922.x
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Maternal 3;13 chromosome insertion, with severe pre-eclampsia.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 17, doi. 10.1111/j.1399-0004.1995.tb03915.x
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Plasma lipids and lipoproteins response to a dietary challenge: analysis of four candidate genes.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 1, doi. 10.1111/j.1399-0004.1995.tb03913.x
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Announcements.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 56, doi. 10.1111/j.1399-0004.1995.tb03923.x
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- Article
Charcot-Marie-Tooth disease: molecular characterization of patients from Central and Southern Italy.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 27, doi. 10.1111/j.1399-0004.1995.tb03917.x
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Dicentric chromosome Y associated with Leydig cell agenesis and sex reversal.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 38, doi. 10.1111/j.1399-0004.1995.tb03919.x
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Increased frequency of the rare PstI allele (P2) in a population of CAD patients in Northern Greece.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 22, doi. 10.1111/j.1399-0004.1995.tb03916.x
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Familial microcephaly with severe neurological deficits: a description of five affected siblings.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 33, doi. 10.1111/j.1399-0004.1995.tb03918.x
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Factors influencing whether or not couples seek genetic counselling: an explorative study in a paediatric surgical unit.
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- Clinical Genetics, 1995, v. 47, n. 1, p. 47, doi. 10.1111/j.1399-0004.1995.tb03921.x
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- Article