The dermatoglyphic pattern of the trisomy 10p syndrome.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 330, doi. 10.1111/j.1399-0004.1978.tb02098.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1978 AND VI 14 AND IP 6
Results: 11
1
2
Urinary tract malformation in the XYY male.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 370, doi. 10.1111/j.1399-0004.1978.tb02104.x
- By:
- Publication type:
- Article
3
Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 345, doi. 10.1111/j.1399-0004.1978.tb02100.x
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- Publication type:
- Article
4
Ketotic hypoglycemia in the Penta X and other chromosome imbalance syndromes.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 367, doi. 10.1111/j.1399-0004.1978.tb02103.x
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- Publication type:
- Article
5
Renal dysplasia and asplenia in two sibs.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 338, doi. 10.1111/j.1399-0004.1978.tb02099.x
- By:
- Publication type:
- Article
6
Polymorphism of apolipoprotein E.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 351, doi. 10.1111/j.1399-0004.1978.tb02101.x
- By:
- Publication type:
- Article
7
Schizophrenia in a North Swedish geographical isolate, 1900-1977. Epidemiology, genetics and biochemistry.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 373, doi. 10.1111/j.1399-0004.1978.tb02105.x
- By:
- Publication type:
- Article
8
European Society of Human Genetics Abstracts from Symposium on 'Chromosome Structure and Function': Vienna, Austria. May 5-7, 1978.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 395, doi. 10.1111/j.1399-0004.1978.tb02106.x
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- Publication type:
- Article
9
Use of microtechniques for the detection of lysosomal enzyme disorders: Tay-Sachs disease, Gm.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 359, doi. 10.1111/j.1399-0004.1978.tb02102.x
- By:
- Publication type:
- Article
10
ABO and Rh phenotyping of foetal blood obtained by foetoscopy.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 324, doi. 10.1111/j.1399-0004.1978.tb02097.x
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- Publication type:
- Article
11
A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphics.
- Published in:
- Clinical Genetics, 1978, v. 14, n. 6, p. 317, doi. 10.1111/j.1399-0004.1978.tb02096.x
- By:
- Publication type:
- Article