Works matching IS 00099163 AND DT 1980 AND VI 17 AND IP 5
Results: 12
Nomenclature of GM2-gangliosidoses.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 320, doi. 10.1111/j.1399-0004.1980.tb00157.x
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- Article
Chromosomal abnormality in Prader-Willi syndrome.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 364, doi. 10.1111/j.1399-0004.1980.tb00164.x
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- Article
Decreasing mosaicism in Down's syndrome.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 335, doi. 10.1111/j.1399-0004.1980.tb00159.x
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- Article
Cardiac involvement in the Cohen syndrome: A case report.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 317, doi. 10.1111/j.1399-0004.1980.tb00156.x
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- Publication type:
- Article
Occurrence of sex chromosome mosaicism and translocation Down's syndrome in the same family.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 341, doi. 10.1111/j.1399-0004.1980.tb00160.x
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- Article
Adult Gmi gangliosidosis: Clinical and biochemical studies on two patients and comparison to other patients called variant or adult Gm1 gangliosidosis.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 323, doi. 10.1111/j.1399-0004.1980.tb00158.x
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- Article
EEC and odontotrichomelic syndromes.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 363, doi. 10.1111/j.1399-0004.1980.tb00163.x
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- Publication type:
- Article
Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 305, doi. 10.1111/j.1399-0004.1980.tb00154.x
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- Article
Announcement.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 367, doi. 10.1111/j.1399-0004.1980.tb00165.x
- Publication type:
- Article
Mental retardation in association with a balanced X-autosome translocation and random inactivation of the X chromosomes.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 309, doi. 10.1111/j.1399-0004.1980.tb00155.x
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- Publication type:
- Article
Cytogenetic evidence for the localisation of the gene for congenital adrenal hyperplasia.
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 349, doi. 10.1111/j.1399-0004.1980.tb00161.x
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- Publication type:
- Article
Concanavalin A reactivity pattern of human amniotic fluid AFP examined by crossed affino-immunoelectrophoresis. A definite test for neural tube defect?
- Published in:
- Clinical Genetics, 1980, v. 17, n. 5, p. 355, doi. 10.1111/j.1399-0004.1980.tb00162.x
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- Publication type:
- Article