Works matching IS 00099163 AND DT 1976 AND VI 9 AND IP 2
Results: 18
Partial trisomy of the long arm of chromosome 7.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 250, doi. 10.1111/j.1399-0004.1976.tb01572.x
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- Article
The inheritance of hyperipoproteinaemia with xanthomatosis:A study of 132 kindreds.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 203, doi. 10.1111/j.1399-0004.1976.tb01569.x
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- Article
Identical tetramelic monodactyly in two brothers.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 143, doi. 10.1111/j.1399-0004.1976.tb01560.x
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- Article
Polycystic kidney disease in a patient with the oral-facial-digital syndrome-Type I.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 183, doi. 10.1111/j.1399-0004.1976.tb01565.x
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- Article
X-linked nonspecific mental retardation:Report of a large kindred.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 125, doi. 10.1111/j.1399-0004.1976.tb01557.x
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- Article
A case of trisomy 20?
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- Clinical Genetics, 1976, v. 9, n. 2, p. 187, doi. 10.1111/j.1399-0004.1976.tb01566.x
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- Article
Cytogenetics of 50 patients with mental retardation and multiple congenital anomalies and 50 normal subjects:Madison blind study IV.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 169, doi. 10.1111/j.1399-0004.1976.tb01564.x
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- Article
Cerebellar ataxia and hypergonadotropic hypogonadism in two kindreds. Chance concurrence, pleiotropism or linkage?
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- Clinical Genetics, 1976, v. 9, n. 2, p. 234, doi. 10.1111/j.1399-0004.1976.tb01570.x
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- Article
Red cell glucose-6-phosphate dehydrogenase deficiency in ethnic groups in Israel.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 131, doi. 10.1111/j.1399-0004.1976.tb01558.x
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- Article
Inheritance of hypoplastic left heart syndrome (HLHS): Further observations.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 245, doi. 10.1111/j.1399-0004.1976.tb01571.x
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- Article
A 45, X woman with a 47, XY, G+ son.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 113, doi. 10.1111/j.1399-0004.1976.tb01555.x
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- Article
Histidinuria: A renal and intestinal histidine transport deficiency found in two mentally retarded children.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 117, doi. 10.1111/j.1399-0004.1976.tb01556.x
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- Article
Autosomal recessive muscular dystrophy in Manitoba Hutterites.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 197, doi. 10.1111/j.1399-0004.1976.tb01568.x
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- Article
An isochromosome of the short arms of the no. 18 chromosome in a mentally retarded girl.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 192, doi. 10.1111/j.1399-0004.1976.tb01567.x
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- Article
48, XXXY Klinefelter syndrome and nail-patella syndrome in the same child.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 163, doi. 10.1111/j.1399-0004.1976.tb01563.x
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- Article
Aplastic anemia followed by leukemia in congenital trisomy 8 mosaicism:Ultrastructural studies of polymorphonuclear cells in peripheral blood.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 134, doi. 10.1111/j.1399-0004.1976.tb01559.x
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- Article
Microphotometry of banded human chromosomes II:Technique for microphotography of banding patterns.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 156, doi. 10.1111/j.1399-0004.1976.tb01562.x
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- Article
Further observations on familial hypobetaliproteinaemia.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 149, doi. 10.1111/j.1399-0004.1976.tb01561.x
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- Article