Biology of presenilins as causative molecules for Alzheimer disease.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 219, doi. 10.1034/j.1399-0004.1999.550401.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1999 AND VI 55 AND IP 4
Results: 14
1
2
HotSpots.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 226, doi. 10.1034/j.1399-0004.1999.550402.x
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- Publication type:
- Article
3
Genetic landmarks through philately – a brief history of diabetes mellitus.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 231, doi. 10.1034/j.1399-0004.1999.550403.x
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- Publication type:
- Article
4
The assent of a nation: genethics and Iceland.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 234, doi. 10.1034/j.1399-0004.1999.550404.x
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- Publication type:
- Article
5
Autosomal dominant cataracts and Peters anomaly in a large Australian family.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 240, doi. 10.1034/j.1399-0004.1999.550405.x
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- Publication type:
- Article
6
Linkage disequilibrium mapping of the Nova Scotia variant of Niemann–Pick disease.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 248, doi. 10.1034/j.1399-0004.1999.550406.x
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- Publication type:
- Article
7
A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysis.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 256, doi. 10.1034/j.1399-0004.1999.550407.x
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- Publication type:
- Article
8
Procedure to protect confidentiality of familial data in community genetics and genomic research.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 259, doi. 10.1034/j.1399-0004.1999.550408.x
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- Publication type:
- Article
9
An unbalanced half-cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence in situ hybridization.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 265, doi. 10.1034/j.1399-0004.1999.550409.x
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- Publication type:
- Article
10
Partial DiGeorge syndrome in two patients with a 10p rearrangement.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 269, doi. 10.1034/j.1399-0004.1999.550410.x
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- Publication type:
- Article
11
Clinical characteristics of Angelman syndrome patients with a non-IC-deleted imprinting mutation.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 277, doi. 10.1034/j.1399-0004.1999.550411.x
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- Publication type:
- Article
12
Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 279, doi. 10.1034/j.1399-0004.1999.550412.x
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- Publication type:
- Article
13
FokI polymorphism at the human vitamin D receptor gene locus in Europeans and Africans.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 281, doi. 10.1034/j.1399-0004.1999.550413.x
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- Publication type:
- Article
14
Tetrasomy 21pter-q22.11: molecular, cytogenetic, and clinical findings.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 283, doi. 10.1034/j.1399-0004.1999.550414.x
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- Publication type:
- Article