Mosaic maternal uniparental isodisomy for chromosome 7q21-qter.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 207, doi. 10.1111/j.1399-0004.2006.00664.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2006 AND VI 70 AND IP 3
Results: 16
1
2
Large genomic alterations in hMSH2 and hMLH1 in early-onset colorectal cancer: identification of a large complex de novo hMLH1 alteration.
- Published in:
- 2006
- By:
- Publication type:
- Letter
3
Caps off: Dkc1 makes the IRESes bloom!
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 195, doi. 10.1111/j.1399-0004.2006.00663_3.x
- By:
- Publication type:
- Article
4
Cryptic mosaicism for monosomy 20 identified in renal tract cells.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 228, doi. 10.1111/j.1399-0004.2006.00652.x
- By:
- Publication type:
- Article
5
A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 233, doi. 10.1111/j.1399-0004.2006.00661.x
- By:
- Publication type:
- Article
6
Applications and limitations of empiric data in provision of recurrence risks for schizophrenia: a practical review for healthcare professionals providing clinical psychiatric genetics consultations.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 177, doi. 10.1111/j.1399-0004.2006.00658.x
- By:
- Publication type:
- Article
7
E-cadherin promoter polymorphism (C-160A) and risk of recurrence in patients with superficial bladder cancer.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 240, doi. 10.1111/j.1399-0004.2006.00666.x
- By:
- Publication type:
- Article
8
Note.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 260, doi. 10.1111/j.1399-0004.2006.00685.x
- Publication type:
- Article
9
Freeman–Sheldon syndrome and Sheldon–Hall syndrome: contracting new genotypes.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 192, doi. 10.1111/j.1399-0004.2006.00663_1.x
- By:
- Publication type:
- Article
10
When bone becomes your enemy: fibrodysplasia ossificans progressiva.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 193, doi. 10.1111/j.1399-0004.2006.00663_2.x
- By:
- Publication type:
- Article
11
Risk-reducing surgery, screening and chemoprevention practices of BRCA1 and BRCA2 mutation carriers: a prospective cohort study.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 198, doi. 10.1111/j.1399-0004.2006.00665.x
- By:
- Publication type:
- Article
12
CYLD mutations underlie Brooke–Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 246, doi. 10.1111/j.1399-0004.2006.00667.x
- By:
- Publication type:
- Article
13
Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1.
- Published in:
- 2006
- By:
- Publication type:
- Letter
14
Genetic and other diseases in the pottery of Tumaco-La Tolita culture in Colombia–Ecuador.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 188, doi. 10.1111/j.1399-0004.2006.00670.x
- By:
- Publication type:
- Article
15
Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 3, p. 214, doi. 10.1111/j.1399-0004.2006.00671.x
- By:
- Publication type:
- Article
16
Hemochromatosis gene mutations in patients with alcoholic cirrhosis.
- Published in:
- 2006
- By:
- Publication type:
- Letter