Apolipoprotein E polymorphism in the Greek population.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 216, doi. 10.1111/j.1399-0004.1997.tb02550.x
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- Publication type:
- Article
Works matching IS 00099163 AND DT 1997 AND VI 52 AND IP 4
Results: 13
1
2
Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 231, doi. 10.1111/j.1399-0004.1997.tb02553.x
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- Publication type:
- Article
3
A Pvull polymorphism detected by a cDNA clone of the gene encoding the human spasmolytic protein (SML1 gene), one of three members of the trefoil peptide gene family clustered on chromosome 21q22.3.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 247, doi. 10.1111/j.1399-0004.1997.tb02556.x
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- Publication type:
- Article
4
Pstl-polymorphism in the human bactericidal permeability increasing protein (BPI) gene.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 249, doi. 10.1111/j.1399-0004.1997.tb02557.x
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- Publication type:
- Article
5
Detection of 100% of the CFTR mutations in 63 CF families from Tyrol.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 240, doi. 10.1111/j.1399-0004.1997.tb02555.x
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- Publication type:
- Article
6
Applicability of a checklist for clinical screening of the fragile X syndrome.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 211, doi. 10.1111/j.1399-0004.1997.tb02549.x
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- Publication type:
- Article
7
Erratum.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 251, doi. 10.1111/j.1399-0004.1997.tb02559.x
- Publication type:
- Article
8
Is the frequency of Robinow syndrome relatively high in Turkey? Four more case reports.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 226, doi. 10.1111/j.1399-0004.1997.tb02552.x
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- Publication type:
- Article
9
Oculocerebrocutaneous syndrome: report of three additional cases and aetiological considerations.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 219, doi. 10.1111/j.1399-0004.1997.tb02551.x
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- Publication type:
- Article
10
Prenatal growth retardation associated with microcephaly, microphthalmos/iris coloboma and other congenital malformations in three siblings.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 250, doi. 10.1111/j.1399-0004.1997.tb02558.x
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- Publication type:
- Article
11
Osteopathia striata with cranial sclerosis: highly variable phenotypic expression within a family.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 199, doi. 10.1111/j.1399-0004.1997.tb02547.x
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- Publication type:
- Article
12
Del (X)(p21.2) in a mother and two daughters with variable ovarian function.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 235, doi. 10.1111/j.1399-0004.1997.tb02554.x
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- Publication type:
- Article
13
Factor V Leiden (R506Q) and risk of venous thromboembolism: a case-control study based on the Spanish population.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 4, p. 206, doi. 10.1111/j.1399-0004.1997.tb02548.x
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- Publication type:
- Article