Association of pre-eclampsia with common coding sequence variations in the lipoprotein lipase gene.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 289, doi. 10.1034/j.1399-0004.1999.560406.x
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- Publication type:
- Article
Works matching IS 00099163 AND DT 1999 AND VI 56 AND IP 4
Results: 15
1
2
Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist?
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 247, doi. 10.1034/j.1399-0004.1999.560401.x
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- Publication type:
- Article
3
The ups and downs of parting COMPany Poly-aspartic acid tract instability: a novel expansion–contraction mutation.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 259, doi. 10.1034/j.1399-0004.1999.560402.x
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- Publication type:
- Article
4
Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 297, doi. 10.1034/j.1399-0004.1999.560407.x
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- Publication type:
- Article
5
Neural stem cells – a versatile tool for cell replacement and gene therapy in the central nervous system.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 267, doi. 10.1034/j.1399-0004.1999.560403.x
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- Publication type:
- Article
6
Growing up without sulfate.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 261, doi. 10.1034/j.1399-0004.1999.560402.1.x
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- Publication type:
- Article
7
A SHOXing new kind of inheritance.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 263, doi. 10.1034/j.1399-0004.1999.560402.2.x
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- Publication type:
- Article
8
FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 282, doi. 10.1034/j.1399-0004.1999.560405.x
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- Publication type:
- Article
9
Genetic landmarks through philately – hemophilia.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 279, doi. 10.1034/j.1399-0004.1999.560404.x
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- Publication type:
- Article
10
Perinatal hypophosphatasia: diagnosis and detection of heterozygote carriers within the family.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 313, doi. 10.1034/j.1399-0004.1999.560409.x
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- Publication type:
- Article
11
‘New’ manifestations of BOR syndrome.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 306, doi. 10.1034/j.1399-0004.1999.560408.x
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- Publication type:
- Article
12
Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 318, doi. 10.1034/j.1399-0004.1999.560410.x
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- Publication type:
- Article
13
Mexican geneticists’ views of ethical issues in genetics testing and screening. Are eugenic principles involved?
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 323, doi. 10.1034/j.1399-0004.1999.560411.x
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- Publication type:
- Article
14
A half cryptic derivative der(18)t(5;18)pat identified by M-FISH and subtelomere probes: clinical findings and review of subtelomeric rearrangements.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 328, doi. 10.1034/j.1399-0004.1999.560412.x
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- Publication type:
- Article
15
Interleukin-4 receptor variant Q576R: ethnic differences and association with atopy.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 333, doi. 10.1034/j.1399-0004.1999.560413.x
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- Publication type:
- Article