Rare SP-A alleles and the SP-A1-6A<sup>4</sup> allele associate with risk for lung carcinoma.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 128, doi. 10.1111/j.1399-0004.2005.00470.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2005 AND VI 68 AND IP 2
Results: 19
1
2
Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism.
- Published in:
- 2005
- By:
- Publication type:
- Letter
3
Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 137, doi. 10.1111/j.1399-0004.2005.00469.x
- By:
- Publication type:
- Article
4
An interaction between the TaqIB polymorphism of cholesterol ester transfer protein and smoking is associated with changes in plasma high-density lipoprotein cholesterol levels in Turks.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 118, doi. 10.1111/j.1399-0004.2005.00467.x
- By:
- Publication type:
- Article
5
A polymorphism in the apolipoprotein A5 gene is associated with weight loss after short-term diet.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 152, doi. 10.1111/j.1399-0004.2005.00463.x
- By:
- Publication type:
- Article
6
Two novel CLN6 mutations in variant late-infantile neuronal ceroid lipofuscinosis patients of Turkish origin.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 167, doi. 10.1111/j.1399-0004.2005.00471.x
- By:
- Publication type:
- Article
7
A putative new locus for an autosomal recessive cerebellar ataxia syndrome on chromosome 22q11.
- Published in:
- 2005
- By:
- Publication type:
- Letter
8
Sitosterolaemia in Switzerland: molecular genetics links the US Amish-Mennonites to their European roots.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 174, doi. 10.1111/j.1399-0004.2005.00472.x
- By:
- Publication type:
- Article
9
Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 146, doi. 10.1111/j.1399-0004.2005.00466.x
- By:
- Publication type:
- Article
10
How lay people respond to messages about genetics, health, and race.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 97, doi. 10.1111/j.1399-0004.2005.00480.x
- By:
- Publication type:
- Article
11
Functional analysis of R75Q mutation in the gene coding for Connexin 26 identified in a family with nonsyndromic hearing loss.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 161, doi. 10.1111/j.1399-0004.2005.00468.x
- By:
- Publication type:
- Article
12
Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart-hand syndrome?
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 155, doi. 10.1111/j.1399-0004.2005.00476.x
- By:
- Publication type:
- Article
13
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation.
- Published in:
- 2005
- By:
- Publication type:
- Letter
14
Genetic regulation of stem cell origins in the mouse embryo.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 2, p. 106, doi. 10.1111/j.1399-0004.2005.00478.x
- By:
- Publication type:
- Article
15
Vertebral anomalies and cartilaginous tracheal sleeve in three patients with Pfeiffer syndrome carrying the S351C FGFR2 mutation.
- Published in:
- 2005
- By:
- Publication type:
- Letter
16
Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism.
- Published in:
- 2005
- By:
- Publication type:
- Letter
17
BBS4 interacts with PCM1.
- Published in:
- 2005
- By:
- Publication type:
- Other
18
A new mutation linked to atrial septal defect.
- Published in:
- 2005
- By:
- Publication type:
- Other
19
Ciliary dysfunction in the Senior–Løken syndrome.
- Published in:
- 2005
- By:
- Publication type:
- Other