Works matching IS 00099163 AND DT 1992 AND VI 41 AND IP 3
Results: 11
Experiences with risk estimates for carriers of chromosomal reciprocal translocations.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 113, doi. 10.1111/j.1399-0004.1992.tb03646.x
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- Article
Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 135, doi. 10.1111/j.1399-0004.1992.tb03649.x
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- Article
A new chromosome 9 variant: an extra band within the 9qh region.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 157, doi. 10.1111/j.1399-0004.1992.tb03654.x
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- Article
The trichorhinophalangeal syndrome with repeated dislocation of the patella.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 139, doi. 10.1111/j.1399-0004.1992.tb03650.x
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Influence of apolipoprotein B signal peptide insertion/deletion polymorphism on serum lipids and apolipoproteins in a Chinese population.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 152, doi. 10.1111/j.1399-0004.1992.tb03653.x
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- Article
Heterogeneity of mutations in Bulgarian phenylketonuria haplotype 1 and 4 alleles.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 123, doi. 10.1111/j.1399-0004.1992.tb03647.x
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- Article
Nonrandom chromosome breakpoints in 6q deletions.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 167, doi. 10.1111/j.1399-0004.1992.tb03656.x
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- Article
Monosomy 6q: report on four new cases.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 159, doi. 10.1111/j.1399-0004.1992.tb03655.x
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- Article
Partial trisomy 19p: case report and natural history.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 143, doi. 10.1111/j.1399-0004.1992.tb03651.x
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- Article
Karyotype/phenotype correlation in females with short stature.
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- Clinical Genetics, 1992, v. 41, n. 3, p. 147, doi. 10.1111/j.1399-0004.1992.tb03652.x
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- Article
Cytogenetic studies of skin fibroblast cultures from a karyotypically normal female with dyskeratosis congenita.
- Published in:
- Clinical Genetics, 1992, v. 41, n. 3, p. 129, doi. 10.1111/j.1399-0004.1992.tb03648.x
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- Article