| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genome-wide approach to identifying novel-imprinted genes
|
Pollard, Katherine S.
|
|
2007
|
122 |
6 |
p. 625-634
|
artikel
|
| 2 |
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p
|
Wessels, Marja W.
|
|
2007
|
122 |
6 |
p. 595-603
|
artikel
|
| 3 |
CFTR mutations and reproductive outcomes in a population isolate
|
Gallego Romero, Irene
|
|
2007
|
122 |
6 |
p. 583-588
|
artikel
|
| 4 |
Discovering DNA: Friedrich Miescher and the early years of nucleic acid research
|
Dahm, Ralf
|
|
2007
|
122 |
6 |
p. 565-581
|
artikel
|
| 5 |
Eberhard Passarge: Color atlas of genetics
|
Dennis, Nicholas Robert
|
|
2007
|
122 |
6 |
p. 665
|
artikel
|
| 6 |
Evidence for linkage of a new region (11p14) to eczema and allergic diseases
|
Guilloud-Bataille, Michel
|
|
2007
|
122 |
6 |
p. 605-614
|
artikel
|
| 7 |
Functional characterization of the human TPH2 5′ regulatory region: untranslated region and polymorphisms modulate gene expression in vitro
|
Chen, Guo-Lin
|
|
2007
|
122 |
6 |
p. 645-657
|
artikel
|
| 8 |
Induction of full-length survival motor neuron by polyphenol botanical compounds
|
Sakla, Mary S.
|
|
2007
|
122 |
6 |
p. 635-643
|
artikel
|
| 9 |
Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14
|
Li, Hui
|
|
2007
|
122 |
6 |
p. 589-593
|
artikel
|
| 10 |
Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy
|
Qin, Minghui
|
|
2007
|
122 |
6 |
p. 615-623
|
artikel
|
| 11 |
Parental transmission of HLA-DRB1*15 in multiple sclerosis
|
Ramagopalan, Sreeram V.
|
|
2007
|
122 |
6 |
p. 661-663
|
artikel
|
| 12 |
Positive association between OLIG2 and schizophrenia in the Chinese Han population
|
Huang, Ke
|
|
2007
|
122 |
6 |
p. 659-660
|
artikel
|
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