Reduced fertility in women with X chromosome abnormality.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 301, doi. 10.1111/j.1399-0004.1984.tb01994.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1984 AND VI 25 AND IP 4
Results: 15
1
2
Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 341, doi. 10.1111/j.1399-0004.1984.tb02001.x
- By:
- Publication type:
- Article
3
Arteriohepatic dysplasia: phenotypic features and family studies.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 323, doi. 10.1111/j.1399-0004.1984.tb01998.x
- By:
- Publication type:
- Article
4
Medical Genetics: 1984. May 10-12, 1984, in Washington, DC.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 378, doi. 10.1111/j.1399-0004.1984.tb02008.x
- By:
- Publication type:
- Article
5
Isolated asternia: an independent entity.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 362, doi. 10.1111/j.1399-0004.1984.tb02005.x
- By:
- Publication type:
- Article
6
Deletion of the long arm of chromosome 11 [46, XX, deI(11)(q24.1 → qter)].
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 373, doi. 10.1111/j.1399-0004.1984.tb02007.x
- By:
- Publication type:
- Article
7
Smith-Lemli-Opitz syndrome in two 46,XY infants with female external genitalia.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 366, doi. 10.1111/j.1399-0004.1984.tb02006.x
- By:
- Publication type:
- Article
8
Polymorphism at the Apoprotein-E locus in relation to risk of coronary disease.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 310, doi. 10.1111/j.1399-0004.1984.tb01995.x
- By:
- Publication type:
- Article
9
Autosomal recessive inheritance of juvenile periodontitis: test of a hypothesis.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 332, doi. 10.1111/j.1399-0004.1984.tb01999.x
- By:
- Publication type:
- Article
10
Fetal mortality in oral cleft families ( V): studies of sporadic vs familial and pure vs syndromic clefts.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 314, doi. 10.1111/j.1399-0004.1984.tb01996.x
- By:
- Publication type:
- Article
11
Cytogenetic and clinical findings in ten 45, X/46, XY patients*.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 336, doi. 10.1111/j.1399-0004.1984.tb02000.x
- By:
- Publication type:
- Article
12
Duplication or insertion in 15q11-13 associated with mental retardation -short stature and obesity - Prader-Willi or Cohen syndrome?
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 347, doi. 10.1111/j.1399-0004.1984.tb02002.x
- By:
- Publication type:
- Article
13
Fetal mortality in oral cleft families (VII): birth intervals.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 318, doi. 10.1111/j.1399-0004.1984.tb01997.x
- By:
- Publication type:
- Article
14
Severe limb malformations in 4p deletion.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 353, doi. 10.1111/j.1399-0004.1984.tb02003.x
- By:
- Publication type:
- Article
15
Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11).
- Published in:
- Clinical Genetics, 1984, v. 25, n. 4, p. 357, doi. 10.1111/j.1399-0004.1984.tb02004.x
- By:
- Publication type:
- Article