| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency
|
Alston, Charlotte L.
|
|
2015
|
134 |
8 |
p. 869-879
|
artikel
|
| 2 |
ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita
|
Abumansour, Iman S.
|
|
2015
|
134 |
8 |
p. 815-822
|
artikel
|
| 3 |
Confronting the missing epistasis problem: on the reproducibility of gene–gene interactions
|
Murk, William
|
|
2015
|
134 |
8 |
p. 837-849
|
artikel
|
| 4 |
Dhavendra Kumar and Charis Eng (eds): Genomic Medicine: Principles and Practice (Oxford Monographs on Medical Genetics) 2nd Edition
|
Christodoulou, John
|
|
2015
|
134 |
8 |
p. 927
|
artikel
|
| 5 |
Diversity of lactase persistence in African milk drinkers
|
Jones, Bryony Leigh
|
|
2015
|
134 |
8 |
p. 917-925
|
artikel
|
| 6 |
Erratum to: The somatic autosomal mutation matrix in cancer genomes
|
Temiz, Nuri A.
|
|
2015
|
134 |
8 |
p. 865-867
|
artikel
|
| 7 |
First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm
|
Luijtgaarden, Koen M. van de
|
|
2015
|
134 |
8 |
p. 881-893
|
artikel
|
| 8 |
Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease
|
Zhang, Xu
|
|
2015
|
134 |
8 |
p. 895-904
|
artikel
|
| 9 |
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up
|
Liu, Fan
|
|
2015
|
134 |
8 |
p. 823-835
|
artikel
|
| 10 |
Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract
|
Hwang, Daw-Yang
|
|
2015
|
134 |
8 |
p. 905-916
|
artikel
|
| 11 |
The somatic autosomal mutation matrix in cancer genomes
|
Temiz, Nuri A.
|
|
2015
|
134 |
8 |
p. 851-864
|
artikel
|
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