| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A biopsy sample reduction approach to identify significant alterations of the testicular transcriptome in the presence of Y-chromosomal microdeletions that are independent of germ cell composition
|
Cappallo-Obermann, Heike
|
|
2010
|
128 |
4 |
p. 421-431
|
artikel
|
| 2 |
Achalasia: will genetic studies provide insights?
|
Gockel, Henning R.
|
|
2010
|
128 |
4 |
p. 353-364
|
artikel
|
| 3 |
Age at onset in Huntington’s disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7
|
Metzger, Silke
|
|
2010
|
128 |
4 |
p. 453-459
|
artikel
|
| 4 |
A homozygous mutation in LTBP2 causes isolated microspherophakia
|
Kumar, Arun
|
|
2010
|
128 |
4 |
p. 365-371
|
artikel
|
| 5 |
Allele-specific recognition of the 3′ splice site of INS intron 1
|
Kralovicova, Jana
|
|
2010
|
128 |
4 |
p. 383-400
|
artikel
|
| 6 |
An approach based on a genome-wide association study reveals candidate loci for narcolepsy
|
Shimada, Mihoko
|
|
2010
|
128 |
4 |
p. 433-441
|
artikel
|
| 7 |
Breakpoint determination of 15 large deletions in Peutz–Jeghers subjects
|
Resta, Nicoletta
|
|
2010
|
128 |
4 |
p. 373-382
|
artikel
|
| 8 |
Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate
|
Wu, Tao
|
|
2010
|
128 |
4 |
p. 401-410
|
artikel
|
| 9 |
Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33
|
Raza, Muhammad Hashim
|
|
2010
|
128 |
4 |
p. 461-463
|
artikel
|
| 10 |
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing
|
Naranjo, Silvia
|
|
2010
|
128 |
4 |
p. 411-419
|
artikel
|
| 11 |
No association between the SNPs (rs3749446 and rs1402000) in the PARL gene and LHON in Chinese patients with m.11778G>A
|
Zhang, A-Mei
|
|
2010
|
128 |
4 |
p. 465-468
|
artikel
|
| 12 |
S.J.L. Knight: Monographs in Human Genetics, Vol. 18, Genetics of Mental Retardation
|
Philip, Nicole
|
|
2010
|
128 |
4 |
p. 469-470
|
artikel
|
| 13 |
Susceptibility to chronic thromboembolic pulmonary hypertension may be conferred by miR-759 via its targeted interaction with polymorphic fibrinogen alpha gene
|
Chen, Zhiyong
|
|
2010
|
128 |
4 |
p. 443-452
|
artikel
|
| 14 |
Walther W., Stein U.S. (eds): Gene therapy of cancer: methods and protocols, 2nd ed
|
Wong, Han Hsi
|
|
2010
|
128 |
4 |
p. 471-472
|
artikel
|
| 15 |
Walther W., Stein U.S. (eds): Gene therapy of cancer: methods and protocols, 2nd ed
|
Wong, Han Hsi
|
|
|
128 |
4 |
p. 471-472
|
artikel
|
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