Works matching IS 00099163 AND DT 1994 AND VI 45 AND IP 4
Results: 13
Clinical aspects of the MASA syndrome in a large family, including expressing females.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 181, doi. 10.1111/j.1399-0004.1994.tb04019.x
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- Article
Effects of consanguinity on anthropometric measurements of newborn infants.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 208, doi. 10.1111/j.1399-0004.1994.tb04025.x
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Announcement.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 219, doi. 10.1111/j.1399-0004.1994.tb04028.x
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- Article
Partial trisomy and monosomy 8p due to inversion duplication.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 203, doi. 10.1111/j.1399-0004.1994.tb04024.x
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- Article
Hereditary pubertal genu valgum in Iran.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 190, doi. 10.1111/j.1399-0004.1994.tb04021.x
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- Article
Achondroplasia with XXY karyotype.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 217, doi. 10.1111/j.1399-0004.1994.tb04027.x
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- Article
The primary hereditary form of distal renal tubular acidosis: clinical and genetic studies in 60-member kindred.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 194, doi. 10.1111/j.1399-0004.1994.tb04022.x
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- Article
Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 165, doi. 10.1111/j.1399-0004.1994.tb04016.x
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- Article
No effect of insertion/ deletion polymorphism at the ACE locus on normal blood pressure level or variability.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 169, doi. 10.1111/j.1399-0004.1994.tb04017.x
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- Article
Multiple coagulation defects and the Cohen syndrome.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 212, doi. 10.1111/j.1399-0004.1994.tb04026.x
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- Article
Prader-Willi-like phenotype in fragile X syndrome.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 175, doi. 10.1111/j.1399-0004.1994.tb04018.x
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- Article
Fragile X syndrome with extra microchromosome.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 186, doi. 10.1111/j.1399-0004.1994.tb04020.x
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- Article
Onychotrichodysplasia and chronic neutropenia without mental retardation (ONS): a second case report.
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- Clinical Genetics, 1994, v. 45, n. 4, p. 200, doi. 10.1111/j.1399-0004.1994.tb04023.x
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- Article