Works matching IS 00099163 AND DT 1999 AND VI 55 AND IP 6
Results: 20
Recombinant proteins for genetic disease.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 389, doi. 10.1034/j.1399-0004.1999.550601.x
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- Publication type:
- Article
HotSpots: The Fat gene.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 395, doi. 10.1034/j.1399-0004.1999.550602.1.x
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- Publication type:
- Article
HotSpots: Neurogenesis challenges age old dogma.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 395, doi. 10.1034/j.1399-0004.1999.550602.2.x
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- Publication type:
- Article
HotSpots: Catch 22.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 396, doi. 10.1034/j.1399-0004.1999.550602.x
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- Publication type:
- Article
40 years of the annual ‘Bar Harbor Course’ (1960–1999): a pictorial history.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 398, doi. 10.1034/j.1399-0004.1999.550603.x
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- Publication type:
- Article
Genetic landmarks through philately – hereditary breast cancer1.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 416, doi. 10.1034/j.1399-0004.1999.550604.x
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- Publication type:
- Article
Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 419, doi. 10.1034/j.1399-0004.1999.550605.x
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- Publication type:
- Article
Chromosome 11q13 and atopic asthma.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 431, doi. 10.1034/j.1399-0004.1999.550606.x
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- Publication type:
- Article
Association between AGT codon 235 polymorphism and variation in serum concentrations of creatinine and urea in Canadian Oji-Cree.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 438, doi. 10.1034/j.1399-0004.1999.550607.x
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- Publication type:
- Article
Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.
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- Clinical Genetics, 1999, v. 55, n. 6, p. 444, doi. 10.1034/j.1399-0004.1999.550608.x
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- Publication type:
- Article
A common truncation variant of lipoprotein lipase (Ser447X) confers protection against coronary heart disease: the Framingham Offspring Study.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 450, doi. 10.1034/j.1399-0004.1999.550609.x
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- Publication type:
- Article
Schizophrenia susceptibility gene locus at Xp22.3.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 455, doi. 10.1034/j.1399-0004.1999.550610.x
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- Publication type:
- Article
Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 461, doi. 10.1034/j.1399-0004.1999.550611.x
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- Publication type:
- Article
Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate gene.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 466, doi. 10.1034/j.1399-0004.1999.550612.x
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- Publication type:
- Article
Further evidence from two families that craniofrontonasal dysplasia maps to Xp22.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 473, doi. 10.1034/j.1399-0004.1999.550613.x
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- Publication type:
- Article
Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 478, doi. 10.1034/j.1399-0004.1999.550614.x
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- Publication type:
- Article
Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 483, doi. 10.1034/j.1399-0004.1999.550615.x
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- Publication type:
- Article
A microdeletion syndrome due to a 3-Mb deletion on 19q13.2 – Diamond–Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 487, doi. 10.1034/j.1399-0004.1999.550616.x
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- Publication type:
- Article
Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocation.
- Published in:
- 1999
- Publication type:
- Letter
Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screening.
- Published in:
- 1999
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- Publication type:
- Letter