Works matching IS 00099163 AND DT 1980 AND VI 17 AND IP 6
Results: 13
Elimination of an abnormal cell line from blood lymphocytes during post-natal growth.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 6, p. 433, doi. 10.1111/j.1399-0004.1980.tb00176.x
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- Article
Genetic association in vitiligo: ABO, MNSs, Rhesus, KeII and Duffy blood groups.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 415, doi. 10.1111/j.1399-0004.1980.tb00172.x
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- Article
A new white forelock (poliosis) syndrome with multiple congenital malformations in two sibs.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 437, doi. 10.1111/j.1399-0004.1980.tb00177.x
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- Article
Hereditary ataxia in a large Danish pedigree.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 385, doi. 10.1111/j.1399-0004.1980.tb00168.x
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- Article
Forsius-Eriksson syndrome: Its relation to the Nettleship-Falls X-linked ocular albinism.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 403, doi. 10.1111/j.1399-0004.1980.tb00170.x
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- Article
The use of genetic linkage in counselling families with dystrophia myotonica.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 443, doi. 10.1111/j.1399-0004.1980.tb00178.x
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- Article
Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 418, doi. 10.1111/j.1399-0004.1980.tb00173.x
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- Article
Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32→13qter.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 428, doi. 10.1111/j.1399-0004.1980.tb00175.x
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- Article
Risk factors associated with neural tube defects.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 394, doi. 10.1111/j.1399-0004.1980.tb00169.x
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- Article
Detection of Lesch-Nyhan Syndrome Carriers: Analysis of hair roots for HPRT by agarose gel electrophoresis and autoradiography.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 369, doi. 10.1111/j.1399-0004.1980.tb00166.x
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- Article
A new case of rearrangement of chromosome 15 associated with Prader Willi syndrome.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 423, doi. 10.1111/j.1399-0004.1980.tb00174.x
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- Article
Kleeblattschadel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24;.
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- Clinical Genetics, 1980, v. 17, n. 6, p. 409, doi. 10.1111/j.1399-0004.1980.tb00171.x
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- Article
The Wolf-Hirschhorn syndrome.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 6, p. 375, doi. 10.1111/j.1399-0004.1980.tb00167.x
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- Article