Infantile XX male: A case report.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 208, doi. 10.1111/j.1399-0004.1976.tb00035.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1976 AND VI 10 AND IP 4
Results: 12
1
2
Multiple non-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects: An autosomal recessive disorder.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 222, doi. 10.1111/j.1399-0004.1976.tb00038.x
- By:
- Publication type:
- Article
3
Letters to the Editor.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 244, doi. 10.1111/j.1399-0004.1976.tb00042.x
- By:
- Publication type:
- Article
4
A familial syndrome of cranial, facial, oral and limb anomalies.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 226, doi. 10.1111/j.1399-0004.1976.tb00039.x
- By:
- Publication type:
- Article
5
Ultrastructural distinct ion of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 245, doi. 10.1111/j.1399-0004.1976.tb00044.x
- By:
- Publication type:
- Article
6
Letters to the Editor.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 244, doi. 10.1111/j.1399-0004.1976.tb00043.x
- By:
- Publication type:
- Article
7
Prenatal diagnosis of 45,X/46,XY mosaicism with postnatal confirmation in a phenotypically normal male infant.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 232, doi. 10.1111/j.1399-0004.1976.tb00040.x
- By:
- Publication type:
- Article
8
Frontonasal dysplasia. Possible hereditary connection with other congenital defects.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 214, doi. 10.1111/j.1399-0004.1976.tb00036.x
- By:
- Publication type:
- Article
9
Clinical studies in benign (Becker type) X-linked muscular dystrophy.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 189, doi. 10.1111/j.1399-0004.1976.tb00033.x
- By:
- Publication type:
- Article
10
A simple, rapid method for prenatal detection of defects in propionate metabolism.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 218, doi. 10.1111/j.1399-0004.1976.tb00037.x
- By:
- Publication type:
- Article
11
X-short arm deletion gonadal dysgenesis in two siblings due to unique translocation (Xp-;16p+).
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 202, doi. 10.1111/j.1399-0004.1976.tb00034.x
- By:
- Publication type:
- Article
12
Alpha-1-antitrypsin (Pi) types in Down's syndrome.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 4, p. 239, doi. 10.1111/j.1399-0004.1976.tb00041.x
- By:
- Publication type:
- Article