3rd lnternatlonal Conference on Thalassemia Sardinia, 3-7 April 1989.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 80, doi. 10.1111/j.1399-0004.1989.tb02910.x
- Publication type:
- Article
Works matching IS 00099163 AND DT 1989 AND VI 35 AND IP 1
Results: 13
1
2
Neural tube defects and omphalocele in trisomy 18.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 77, doi. 10.1111/j.1399-0004.1989.tb02908.x
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- Publication type:
- Article
3
Emery-Dreifuss syndrome and X-linked muscular dystrophy with contractures: evidence for homogeneity.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 1, doi. 10.1111/j.1399-0004.1989.tb02898.x
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- Publication type:
- Article
4
Molecular Xp deletion in a male: suggestion of a locus for hypogonadotropic hypogonadism distal to the glycerol kinase and adrenal hypoplasia loci.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 5, doi. 10.1111/j.1399-0004.1989.tb02899.x
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- Publication type:
- Article
5
The motivation of at-risk individuals and their partners in deciding for or against predictive testing for Huntington's disease.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 29, doi. 10.1111/j.1399-0004.1989.tb02902.x
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- Publication type:
- Article
6
Growth, bone maturation and pubertal development in children with the EMG-syndrome.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 20, doi. 10.1111/j.1399-0004.1989.tb02901.x
- By:
- Publication type:
- Article
7
Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneity.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 13, doi. 10.1111/j.1399-0004.1989.tb02900.x
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- Publication type:
- Article
8
Alpha-fetoprotein findings in a case of cystic adenomatoid malformation of the lung.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 75, doi. 10.1111/j.1399-0004.1989.tb02907.x
- By:
- Publication type:
- Article
9
Bloom's Syndrome. XII. Report from the Registry for 1987.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 57, doi. 10.1111/j.1399-0004.1989.tb02905.x
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- Publication type:
- Article
10
A case of prenatal diagnosis of a familial satellited Yq chromosome.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 70, doi. 10.1111/j.1399-0004.1989.tb02906.x
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- Publication type:
- Article
11
Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation?
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 41, doi. 10.1111/j.1399-0004.1989.tb02903.x
- By:
- Publication type:
- Article
12
'Unstable' translocation not proven unstable.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 78, doi. 10.1111/j.1399-0004.1989.tb02909.x
- By:
- Publication type:
- Article
13
DNA polymorphism at the locus for human cholesteryl ester transfer protein (CETP) is associated with high density lipoprotein cholesterol and apolipoprotein levels.
- Published in:
- Clinical Genetics, 1989, v. 35, n. 1, p. 49, doi. 10.1111/j.1399-0004.1989.tb02904.x
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- Publication type:
- Article