The genetics of osteoporosis: ‘complexities and difficulties’.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 161, doi. 10.1034/j.1399-0004.2000.570301.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2000 AND VI 57 AND IP 3
Results: 14
1
2
Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 232, doi. 10.1034/j.1399-0004.2000.570311.x
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- Publication type:
- Article
3
Rett syndrome: The influence of dysregulated gene slicing.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 170, doi. 10.1034/j.1399-0004.2000.570302.x
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- Publication type:
- Article
4
Molecular analysis of the 5′-flanking region of the neurofibromatosis type 1 (NF1) gene: identification of five sequence variants.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 221, doi. 10.1034/j.1399-0004.2000.570308.x
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- Publication type:
- Article
5
Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemia.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 225, doi. 10.1034/j.1399-0004.2000.570309.x
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- Publication type:
- Article
6
Involvement of an inflammation-related gene in X-linked mental retardation.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 171, doi. 10.1034/j.1399-0004.2000.570302.1.x
- By:
- Publication type:
- Article
7
Breaking the law: the molecular basis of non-Mendelian transmission.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 173, doi. 10.1034/j.1399-0004.2000.570302.2.x
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- Publication type:
- Article
8
Comparison of the role of dopamine, serotonin, and noradrenaline genes in ADHD, ODD and conduct disorder: multivariate regression analysis of 20 genes.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 178, doi. 10.1034/j.1399-0004.2000.570304.x
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- Publication type:
- Article
9
Xolótl: god of monstrosities.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 176, doi. 10.1034/j.1399-0004.2000.570303.x
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- Publication type:
- Article
10
A pilot study of the possible role of familial defects in anticoagulation as a cause for terminal limb reduction malformations.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 197, doi. 10.1034/j.1399-0004.2000.570305.x
- By:
- Publication type:
- Article
11
A germline mutation at the extreme 3′ end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 205, doi. 10.1034/j.1399-0004.2000.570306.x
- By:
- Publication type:
- Article
12
A rapid fluorescent multiplexed-PCR analysis (FMPA) for founder mutations in the BRCA1 and BRCA2 genes.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 213, doi. 10.1034/j.1399-0004.2000.570307.x
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- Publication type:
- Article
13
Spina bifida and common mutations at the homocysteine metabolism pathway.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 230, doi. 10.1034/j.1399-0004.2000.570310.x
- By:
- Publication type:
- Article
14
Identification of cystic fibrosis mutations in Oman.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 235, doi. 10.1034/j.1399-0004.2000.570312.x
- By:
- Publication type:
- Article