Clinically manifesting carriers in Duchenne muscular dystrophy.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 6, doi. 10.1111/j.1399-0004.1981.tb01799.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1981 AND VI 20 AND IP 1
Results: 15
1
2
46,XY/48,XXY,+8 in a male with clinical and dermatoglyphic features of mosaic trisomy 8 syndrome.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 60, doi. 10.1111/j.1399-0004.1981.tb01808.x
- By:
- Publication type:
- Article
3
Cleft palate: A genetic and epidemiologic investigation.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 13, doi. 10.1111/j.1399-0004.1981.tb01800.x
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- Publication type:
- Article
4
Urinary amino acids and organic acids in the Sjögren-Larsson syndrome.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 64, doi. 10.1111/j.1399-0004.1981.tb01809.x
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- Publication type:
- Article
5
Gonadal dysgenesis, intra-X chromosome insertion, and possible position effect in an otherwise normal female.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 28, doi. 10.1111/j.1399-0004.1981.tb01802.x
- By:
- Publication type:
- Article
6
A new growth deficiency syndrome.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 1, doi. 10.1111/j.1399-0004.1981.tb01798.x
- By:
- Publication type:
- Article
7
Phenotypic variation in Meckel syndrome.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 74, doi. 10.1111/j.1399-0004.1981.tb01811.x
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- Publication type:
- Article
8
Adrenal adenomas in a patient with Gardner's syndrome.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 67, doi. 10.1111/j.1399-0004.1981.tb01810.x
- By:
- Publication type:
- Article
9
'Fragile X' Chromosome in Normal Males.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 78, doi. 10.1111/j.1399-0004.1981.tb01812.x
- By:
- Publication type:
- Article
10
Familial 5/14 translocation with triple X and 47,XY + 14q-.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 40, doi. 10.1111/j.1399-0004.1981.tb01804.x
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- Publication type:
- Article
11
Polymorphism in chromosome 4.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 44, doi. 10.1111/j.1399-0004.1981.tb01805.x
- By:
- Publication type:
- Article
12
Sanfilippo syndrome type C: assay for acetyl-CoA: α-glucosaminide N-acetyltransferase in leukocytes for detection of homozygous and heterozygous individuals.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 55, doi. 10.1111/j.1399-0004.1981.tb01807.x
- By:
- Publication type:
- Article
13
Follow-up of 32 children with autosomal translocations found among 11,148 consecutively newborn children from 1969 to 1974.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 48, doi. 10.1111/j.1399-0004.1981.tb01806.x
- By:
- Publication type:
- Article
14
An Indian family with postaxial Polydactyly in four generations.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 36, doi. 10.1111/j.1399-0004.1981.tb01803.x
- By:
- Publication type:
- Article
15
Dominant inheritance of microcephaly with short stature.
- Published in:
- Clinical Genetics, 1981, v. 20, n. 1, p. 25, doi. 10.1111/j.1399-0004.1981.tb01801.x
- By:
- Publication type:
- Article