Fragile sites in human chromosomes I The effect of methionine on the Xq fragile site.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 228, doi. 10.1111/j.1399-0004.1981.tb00703.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1981 AND VI 19 AND IP 4
Results: 15
1
2
X-linked Dyggve-Melchior-Clausen Syndrome.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 304, doi. 10.1111/j.1399-0004.1981.tb00714.x
- By:
- Publication type:
- Article
3
A twin study of aryl hydrocarbon hydroxylase (AHH) inducibility in cultured lymphocytes.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 281, doi. 10.1111/j.1399-0004.1981.tb00710.x
- By:
- Publication type:
- Article
4
An unusual form of metachromatic leukodystrophy in three siblings.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 222, doi. 10.1111/j.1399-0004.1981.tb00702.x
- By:
- Publication type:
- Article
5
Turner's syndrome and 45, XO/46, X, del(X)(p11p22) karyotype.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 262, doi. 10.1111/j.1399-0004.1981.tb00706.x
- By:
- Publication type:
- Article
6
Sjögren-Larsson syndrome in Sweden. A clinical, genetic and epidemiological study.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 233, doi. 10.1111/j.1399-0004.1981.tb00704.x
- By:
- Publication type:
- Article
7
HLA Phenotypes and joint affection in psoriasis, acute anterior uveitis and chronic prostatitis.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 266, doi. 10.1111/j.1399-0004.1981.tb00707.x
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- Publication type:
- Article
8
Concanavalin A Reactivity of Human Amniotic Fluid AFP.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 302, doi. 10.1111/j.1399-0004.1981.tb00713.x
- By:
- Publication type:
- Article
9
45, X Constitution in a H-Y antigen positive boy with partial monosomy 5p.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 290, doi. 10.1111/j.1399-0004.1981.tb00711.x
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- Publication type:
- Article
10
ECG Conduction disturbance in the first-degree relatives of children with ventricular septal defect.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 298, doi. 10.1111/j.1399-0004.1981.tb00712.x
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- Publication type:
- Article
11
Announcement.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 305, doi. 10.1111/j.1399-0004.1981.tb00715.x
- Publication type:
- Article
12
Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis).
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 271, doi. 10.1111/j.1399-0004.1981.tb00708.x
- By:
- Publication type:
- Article
13
Huntington's Chorea in South Wales A genetic and epidemiological study.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 213, doi. 10.1111/j.1399-0004.1981.tb00701.x
- By:
- Publication type:
- Article
14
Venous thromboembolic disease in Klinefelter's syndrome.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 275, doi. 10.1111/j.1399-0004.1981.tb00709.x
- By:
- Publication type:
- Article
15
Increased amnionic fluid alpha-fetoprotein due to a holoacardium amorphous twin.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 4, p. 257, doi. 10.1111/j.1399-0004.1981.tb00705.x
- By:
- Publication type:
- Article