Found: 13
Select item for more details and to access through your institution.
Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 82, doi. 10.1038/sj.ejhg.5200583
- By:
- Publication type:
- Article
A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 121, doi. 10.1038/sj.ejhg.5200585
- By:
- Publication type:
- Article
Attempts to detect retrotransposition and de novo deletion of Alus and other dispersed repeats at specific loci in the human genome.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 143, doi. 10.1038/sj.ejhg.5200590
- By:
- Publication type:
- Article
PCAP is the major known prostate cancer predisposing locus in families from south and west Europe.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 135, doi. 10.1038/sj.ejhg.5200592
- By:
- Publication type:
- Article
Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 105
- By:
- Publication type:
- Article
The impact of genotyping error on family-based analysis of quantitative traits.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 130, doi. 10.1038/sj.ejhg.5200594
- By:
- Publication type:
- Article
XLMR genes: update 2000.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 71, doi. 10.1038/sj.ejhg.5200603
- By:
- Publication type:
- Article
Letter.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 150, doi. 10.1038/sj.ejhg.5200611
- By:
- Publication type:
- Article
Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 97, doi. 10.1038/sj.ejhg.5200597
- By:
- Publication type:
- Article
Premature termination mutations in exon 3 of the SMN1 gene are associated with exon skipping and a relatively mild SMA phenotype.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 113, doi. 10.1038/sj.ejhg.5200599
- By:
- Publication type:
- Article
Maternally inherited deafness associated with a T1095C mutation in the mDNA.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 147, doi. 10.1038/sj.ejhg.5200601
- By:
- Publication type:
- Article
Letter.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 151, doi. 10.1038/sj.ejhg.5200596
- By:
- Publication type:
- Article
Human α-N-acetylgalactosaminidase (α-NAGA) deficiency: no association with neuroaxonal dystrophy?
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 91, doi. 10.1038/sj.ejhg.5200598
- By:
- Publication type:
- Article