Hirschsprung's disease and Ondine's curse: further evidence for a distinct syndrome.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 200, doi. 10.1111/j.1399-0004.1989.tb03189.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1989 AND VI 36 AND IP 3
Results: 12
1
2
Tandem Y/6 translocation with partial deletion 6 (p23→pter).
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 204, doi. 10.1111/j.1399-0004.1989.tb03190.x
- By:
- Publication type:
- Article
3
Parental origin of chromosomal non-disjunction in a 49,XXXXY male using recombinant-DNA techniques.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 152, doi. 10.1111/j.1399-0004.1989.tb03181.x
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- Publication type:
- Article
4
Announcement.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 208, doi. 10.1111/j.1399-0004.1989.tb03191.x
- Publication type:
- Article
5
Macrosomia, microphthalmia, ± cleft palate and early infant death: a new autosomal recessive syndrome.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 174, doi. 10.1111/j.1399-0004.1989.tb03184.x
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- Publication type:
- Article
6
Application of the anthropometric discriminant functions in estimation of carrier probabilities in Martin-Bell syndrome.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 145, doi. 10.1111/j.1399-0004.1989.tb03180.x
- By:
- Publication type:
- Article
7
Mental illness and cognition in relation to age at puberty: a hypothesis.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 156, doi. 10.1111/j.1399-0004.1989.tb03182.x
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- Publication type:
- Article
8
Two rare cases of 6p partial deletion.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 196, doi. 10.1111/j.1399-0004.1989.tb03188.x
- By:
- Publication type:
- Article
9
The contribution of H LA to rheumatoid arthritis.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 178, doi. 10.1111/j.1399-0004.1989.tb03185.x
- By:
- Publication type:
- Article
10
Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 189, doi. 10.1111/j.1399-0004.1989.tb03187.x
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- Publication type:
- Article
11
Increased frequencies of apolipoprotein ε2 and ε4 alleles in patients with ischemic heart disease.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 183, doi. 10.1111/j.1399-0004.1989.tb03186.x
- By:
- Publication type:
- Article
12
The effect of consanguinity on the reproductive wastage in the Turkish population.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 3, p. 168, doi. 10.1111/j.1399-0004.1989.tb03183.x
- By:
- Publication type:
- Article