Works matching IS 00099163 AND DT 1982 AND VI 21 AND IP 3
Results: 12
International Registry of Abnormal Karyotypes. A Repository of Chromosomal Variants and Anomalies in Man: current status.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 222, doi. 10.1111/j.1399-0004.1982.tb00967.x
- By:
- Publication type:
- Article
HLA antigens, psoriasis and acute anterior uveitis in Bechterew's syndrome (ankylosing spondylitis).
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 215, doi. 10.1111/j.1399-0004.1982.tb00966.x
- By:
- Publication type:
- Article
The atrioventricular conduction time - a heritable trait?: III Twin studies.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 181, doi. 10.1111/j.1399-0004.1982.tb00960.x
- By:
- Publication type:
- Article
Hereditary pyrophosphate arthropathy (familial articular chondrocalcinosis) in Sweden.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 174, doi. 10.1111/j.1399-0004.1982.tb00959.x
- By:
- Publication type:
- Article
Degradation of keratan sulfate by ß-N-acetylhexosaminidases in GM.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 196, doi. 10.1111/j.1399-0004.1982.tb00963.x
- By:
- Publication type:
- Article
Testicular feminization syndrome (TFS) associated with paragonadal cysts.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 203, doi. 10.1111/j.1399-0004.1982.tb00964.x
- By:
- Publication type:
- Article
SCE in Bloom syndrome B and T lymphocytes.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 184, doi. 10.1111/j.1399-0004.1982.tb00961.x
- By:
- Publication type:
- Article
Preliminary Announcement.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 224, doi. 10.1111/j.1399-0004.1982.tb00968.x
- Publication type:
- Article
Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 161, doi. 10.1111/j.1399-0004.1982.tb00957.x
- By:
- Publication type:
- Article
Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and deletion 10q.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 187, doi. 10.1111/j.1399-0004.1982.tb00962.x
- By:
- Publication type:
- Article
Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 209, doi. 10.1111/j.1399-0004.1982.tb00965.x
- By:
- Publication type:
- Article
An unusual connective tissue disease in mother and son: A 'new' type of Ehlers-Danlos syndrome?
- Published in:
- Clinical Genetics, 1982, v. 21, n. 3, p. 168, doi. 10.1111/j.1399-0004.1982.tb00958.x
- By:
- Publication type:
- Article