Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 107, doi. 10.1111/j.1399-0004.2004.00329.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2005 AND VI 67 AND IP 2
Results: 12
1
2
The potential impact of genetic counseling for mental illness.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 134, doi. 10.1111/j.1399-0004.2004.00330.x
- By:
- Publication type:
- Article
3
Multiplex ligation-dependent probe amplification is superior for detecting deletions/duplications in Duchenne muscular dystrophy.
- Published in:
- 2005
- By:
- Publication type:
- Letter
4
Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 160, doi. 10.1111/j.1399-0004.2004.00386.x
- By:
- Publication type:
- Article
5
Compound heterozygosity for two non-synonymous polymorphisms inNPC1L1in a non-responder to ezetimibe.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 175, doi. 10.1111/j.1399-0004.2004.00388.x
- By:
- Publication type:
- Article
6
Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosis.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 166, doi. 10.1111/j.1399-0004.2004.00389.x
- By:
- Publication type:
- Article
7
A novel microdeletion syndrome with loss of theMSH2locus and hereditary non-polyposis colorectal cancer.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 178, doi. 10.1111/j.1399-0004.2004.00390.x
- By:
- Publication type:
- Article
8
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 183, doi. 10.1111/j.1399-0004.2004.00391.x
- By:
- Publication type:
- Article
9
The vast array of opportunity for genomic discovery in human genetic disorders.
- Published in:
- 2005
- By:
- Publication type:
- Other
10
Higher resolution solutions for mapping the mystery of idiopathic intellectual disability.
- Published in:
- 2005
- Publication type:
- Other
11
A new frontier for fetal diagnosis using genomic CGH microarrays.
- Published in:
- 2005
- Publication type:
- Other
12
The developing limb and the control of the number of digits.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 2, p. 143, doi. 10.1111/j.1399-0004.2005.00404.x
- By:
- Publication type:
- Article