A family of mammalian anion transporters and their involvement in human genetic diseases.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1883, doi. 10.1093/hmg/8.10.1883
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 1999 AND VI 8 AND IP 10
Results: 17
1
2
Williams-Beuren syndrome: genes and mechanisms.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1947, doi. 10.1093/hmg/8.10.1947
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- Publication type:
- Article
3
The limb-girdle muscular dystrophies--multiple genes, multiple mechanisms.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1875, doi. 10.1093/hmg/8.10.1875
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- Publication type:
- Article
4
Ataxic mouse mutants and molecular mechanisms of absence epilepsy.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1907, doi. 10.1093/hmg/8.10.1907
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- Publication type:
- Article
5
Osteopetrosis and osteoporosis: two sides of the same coin.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1839, doi. 10.1093/hmg/8.10.1839
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- Publication type:
- Article
6
Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1833, doi. 10.1093/hmg/8.10.1833
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- Publication type:
- Article
7
Autosomal dominant polycystic kidney disease: clues to pathogenesis.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1861, doi. 10.1093/hmg/8.10.1861
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- Publication type:
- Article
8
Computational methods for the identification of differential and coordinated gene expression.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1821, doi. 10.1093/hmg/8.10.1821
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- Publication type:
- Article
9
The genetics of disorders with synuclein pathology and parkinsonism.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1901, doi. 10.1093/hmg/8.10.1901
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- Publication type:
- Article
10
Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1847, doi. 10.1093/hmg/8.10.1847
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- Publication type:
- Article
11
Towards a molecular understanding of Prader-Willi and Angelman syndromes.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1867, doi. 10.1093/hmg/8.10.1867
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- Publication type:
- Article
12
Nonsense-mediated mRNA decay in health and disease.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1893, doi. 10.1093/hmg/8.10.1893
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- Publication type:
- Article
13
Molecular genetics of the Finnish disease heritage.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1913, doi. 10.1093/hmg/8.10.1913
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- Publication type:
- Article
14
Forward genetics in mammalian cells: functional approaches to gene discovery.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1925, doi. 10.1093/hmg/8.10.1925
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- Publication type:
- Article
15
Mouse ENU Mutagenesis.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1955, doi. 10.1093/hmg/8.10.1955
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- Publication type:
- Article
16
Genetics of HIV-1 infection: chemokine receptor CCR5 polymorphism and its consequences.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1939, doi. 10.1093/hmg/8.10.1939
- By:
- Publication type:
- Article
17
The many faces and factors of orofacial clefts.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 10, p. 1853, doi. 10.1093/hmg/8.10.1853
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- Publication type:
- Article