Works matching IS 00099163 AND DT 1981 AND VI 19 AND IP 3
Results: 14
Klinefelter's syndrome with a 47, XXY, inv (12) (q15q24) karyotype.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 188, doi. 10.1111/j.1399-0004.1981.tb00694.x
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- Article
HLA profile and Reiter's syndrome.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 159, doi. 10.1111/j.1399-0004.1981.tb00690.x
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- Article
Prenatal diagnosis of campomelic dwarfism.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 199, doi. 10.1111/j.1399-0004.1981.tb00696.x
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- Article
Trisomy 6qter.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 3, p. 202, doi. 10.1111/j.1399-0004.1981.tb00697.x
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Letter to the Editors.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 3, p. 209, doi. 10.1111/j.1399-0004.1981.tb00699.x
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Increased frequencies of chromosomal abnormalities in families with a history of fetal wastage.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 168, doi. 10.1111/j.1399-0004.1981.tb00691.x
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- Article
An XXXY boy with X/XY half-sister.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 181, doi. 10.1111/j.1399-0004.1981.tb00693.x
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- Article
Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 174, doi. 10.1111/j.1399-0004.1981.tb00692.x
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- Article
Variation in nucleolar organizer activity in lymphocytes of females with adenocarcinoma.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 145, doi. 10.1111/j.1399-0004.1981.tb00687.x
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Pregnancy in Bloom's Syndrome.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 156, doi. 10.1111/j.1399-0004.1981.tb00689.x
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- Article
Familial tricho-rhino-phalangeal syndrome Type II.
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- Clinical Genetics, 1981, v. 19, n. 3, p. 149, doi. 10.1111/j.1399-0004.1981.tb00688.x
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Announcements.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 3, p. 210, doi. 10.1111/j.1399-0004.1981.tb00700.x
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- Article
Orbital cyst in addition to congenital cerebral and focal dermal malformations: A new entity?
- Published in:
- Clinical Genetics, 1981, v. 19, n. 3, p. 191, doi. 10.1111/j.1399-0004.1981.tb00695.x
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- Article
Normal Hageman factor level in 7q deletion syndrome.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 3, p. 207, doi. 10.1111/j.1399-0004.1981.tb00698.x
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- Article