Found: 12
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The Dyggve-Melchior-Clausen syndrome in Indian siblings.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 240, doi. 10.1111/j.1399-0004.1992.tb03248.x
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- Article
β-Thalassaemia mutations and their linkage to β-haplotypes in Tamil Nadu in Southern India.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 251, doi. 10.1111/j.1399-0004.1992.tb03250.x
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- Publication type:
- Article
Detection of the Pro.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 273, doi. 10.1111/j.1399-0004.1992.tb03255.x
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- Article
Deletion of 15q12 in Angelman syndrome: report of 3 new cases.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 229, doi. 10.1111/j.1399-0004.1992.tb03246.x
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- Article
Analysis of three glucose transporter genes in a Caucasian population: no associations with non-insulin-dependent diabetes and obesity.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 260, doi. 10.1111/j.1399-0004.1992.tb03252.x
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- Publication type:
- Article
Deletion ΔF508 and clinical expression of cystic fibrosis-related liver disease.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 271, doi. 10.1111/j.1399-0004.1992.tb03254.x
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- Publication type:
- Article
A new polymorphism in exon 11 of the LDL receptor gene in healthy people and in familial hypercholesterolemia subjects.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 224, doi. 10.1111/j.1399-0004.1992.tb03245.x
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- Publication type:
- Article
De novo interstitial deletion 16(q12. 1q13) of paternal origin in a 10-year-old boy.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 246, doi. 10.1111/j.1399-0004.1992.tb03249.x
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- Publication type:
- Article
A case of human chimerism detected by unbalanced chromosomal translocation.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 257, doi. 10.1111/j.1399-0004.1992.tb03251.x
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- Article
Fertility in myotonic dystrophy in Saguenay-Lac-St-Jean: a historical perspective.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 234, doi. 10.1111/j.1399-0004.1992.tb03247.x
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- Publication type:
- Article
Deciphering the fluorescent variability of human genomic heterochromatin by DA/DAPI technique.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 267, doi. 10.1111/j.1399-0004.1992.tb03253.x
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- Publication type:
- Article
StyI polymorphism in an enhancer region of the second intron of the apolipoprotein B gene in hyper- and hypocholesterolemic subjects.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 217, doi. 10.1111/j.1399-0004.1992.tb03244.x
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- Publication type:
- Article