No 'fragile X' chromosome in normal men.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 140, doi. 10.1111/j.1399-0004.1981.tb00685.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1981 AND VI 19 AND IP 2
Results: 12
1
2
Muscular anomalies caused by delayed development in human aneuploidy.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 111, doi. 10.1111/j.1399-0004.1981.tb00679.x
- By:
- Publication type:
- Article
3
Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter).
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 122, doi. 10.1111/j.1399-0004.1981.tb00681.x
- By:
- Publication type:
- Article
4
A biastellited marker chromosome in an infant with the caudal regression anomalad.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 126, doi. 10.1111/j.1399-0004.1981.tb00682.x
- By:
- Publication type:
- Article
5
Clinical and neurophysiological findings in heterozygotes for nonketotic hyperglycinemia.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 94, doi. 10.1111/j.1399-0004.1981.tb00677.x
- By:
- Publication type:
- Article
6
49, XYYYY. A case report.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 87, doi. 10.1111/j.1399-0004.1981.tb00676.x
- By:
- Publication type:
- Article
7
Announcements.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 142, doi. 10.1111/j.1399-0004.1981.tb00686.x
- Publication type:
- Article
8
Athelia in a female infant heterozygous for anhidrotic ectodermal dysplasia.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 117, doi. 10.1111/j.1399-0004.1981.tb00680.x
- By:
- Publication type:
- Article
9
Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24).
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 130, doi. 10.1111/j.1399-0004.1981.tb00683.x
- By:
- Publication type:
- Article
10
Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 101, doi. 10.1111/j.1399-0004.1981.tb00678.x
- By:
- Publication type:
- Article
11
A recognizable phenotype in a child with partial duplication 13q in a family with t(10q;13q).
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 81, doi. 10.1111/j.1399-0004.1981.tb00675.x
- By:
- Publication type:
- Article
12
α.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 2, p. 134, doi. 10.1111/j.1399-0004.1981.tb00684.x
- By:
- Publication type:
- Article