Structural abnormalities of the Y-chromosome and craniosynostosis.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 100, doi. 10.1111/j.1399-0004.1992.tb03148.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1992 AND VI 42 AND IP 2
Results: 11
1
2
X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible male.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 76, doi. 10.1111/j.1399-0004.1992.tb03143.x
- By:
- Publication type:
- Article
3
Ring Y chromosome: cytogenetic and molecular characterization.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 71, doi. 10.1111/j.1399-0004.1992.tb03142.x
- By:
- Publication type:
- Article
4
Association of haptoglobin types with serum lipids and apolipoproteins in a Chinese population.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 57, doi. 10.1111/j.1399-0004.1992.tb03140.x
- By:
- Publication type:
- Article
5
Occipital scalp defect associated with valvular pulmonary stenosis. A new entity?
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 97, doi. 10.1111/j.1399-0004.1992.tb03147.x
- By:
- Publication type:
- Article
6
MASA syndrome.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 102, doi. 10.1111/j.1399-0004.1992.tb03150.x
- By:
- Publication type:
- Article
7
EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 101, doi. 10.1111/j.1399-0004.1992.tb03149.x
- By:
- Publication type:
- Article
8
Y-derived sequence detected in minute chromosomes by polymerase chain reaction and in situ hybridization.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 80, doi. 10.1111/j.1399-0004.1992.tb03144.x
- By:
- Publication type:
- Article
9
Typical and partial cat eye syndrome: identification of the marker chromosome by FISH.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 91, doi. 10.1111/j.1399-0004.1992.tb03146.x
- By:
- Publication type:
- Article
10
A novel truncated apolipoprotein B (apo B55) in a patient with familial hypobetalipo-proteinemia and atypical retinitis pigmentosa.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 62, doi. 10.1111/j.1399-0004.1992.tb03141.x
- By:
- Publication type:
- Article
11
A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH).
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 84, doi. 10.1111/j.1399-0004.1992.tb03145.x
- By:
- Publication type:
- Article