Works matching IS 00099163 AND DT 1980 AND VI 18 AND IP 6
Results: 16
Osteopathia striata with cranial sclerosis: Highly variable expression within a family including cleft palate in two neonatal cases.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 6, p. 462, doi. 10.1111/j.1399-0004.1980.tb01795.x
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- Article
The use of probability trees in genetic counselling.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 408, doi. 10.1111/j.1399-0004.1980.tb01784.x
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- Article
Atrioventricular conduction time -a heritable trait?
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- Clinical Genetics, 1980, v. 18, n. 6, p. 450, doi. 10.1111/j.1399-0004.1980.tb01792.x
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- Article
Sotos syndrome in two brothers.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 421, doi. 10.1111/j.1399-0004.1980.tb01787.x
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- Article
Atrioventricular conduction time - a heritable trait?
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- Clinical Genetics, 1980, v. 18, n. 6, p. 454, doi. 10.1111/j.1399-0004.1980.tb01793.x
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- Article
Complex chromosome rearrangements:Report of a new case and literature review.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 436, doi. 10.1111/j.1399-0004.1980.tb01790.x
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- Article
Announcements.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 476, doi. 10.1111/j.1399-0004.1980.tb01797.x
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- Article
Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11←q13) segment of chromosome 2.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 402, doi. 10.1111/j.1399-0004.1980.tb01783.x
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- Article
Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 6, p. 413, doi. 10.1111/j.1399-0004.1980.tb01785.x
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- Article
A possible reason for clustering of trisomy 18 in humans.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 475, doi. 10.1111/j.1399-0004.1980.tb01796.x
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- Article
Hereditary urogenital adysplasia.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 417, doi. 10.1111/j.1399-0004.1980.tb01786.x
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- Article
Ring chromosome 15 in a male adult with radial defects. Evaluation of the phenotype.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 428, doi. 10.1111/j.1399-0004.1980.tb01788.x
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- Article
Prenatal diagnosis of a de novo reciprocal translocation 46,XX,t(1;18) (p22;q23).
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- Clinical Genetics, 1980, v. 18, n. 6, p. 434, doi. 10.1111/j.1399-0004.1980.tb01789.x
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- Article
Familial occurrence of chromosome 7/12 translocation.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 445, doi. 10.1111/j.1399-0004.1980.tb01791.x
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- Article
Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter.
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- Clinical Genetics, 1980, v. 18, n. 6, p. 456, doi. 10.1111/j.1399-0004.1980.tb01794.x
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- Article
The campomelic syndrome in a singleton and monozygotic twins.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 6, p. 397, doi. 10.1111/j.1399-0004.1980.tb01782.x
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- Article