| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations
|
Hatchell, Kathryn E.
|
|
2019
|
138 |
10 |
p. 1155-1169
|
artikel
|
| 2 |
A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss
|
Sineni, Claire J.
|
|
2019
|
138 |
10 |
p. 1071-1075
|
artikel
|
| 3 |
Autosomal recessive diseases among the Israeli Arabs
|
Zlotogora, Joël
|
|
2019
|
138 |
10 |
p. 1117-1122
|
artikel
|
| 4 |
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans
|
Kitzler, Thomas M.
|
|
2019
|
138 |
10 |
p. 1105-1115
|
artikel
|
| 5 |
Correction to: Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic histories
|
Ceballos, Francisco C.
|
|
2019
|
138 |
10 |
p. 1143-1144
|
artikel
|
| 6 |
Genetic associations of breast and prostate cancer are enriched for regulatory elements identified in disease-related tissues
|
Chen, Hongjie
|
|
2019
|
138 |
10 |
p. 1091-1104
|
artikel
|
| 7 |
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates
|
Ouyang, Qing
|
|
2019
|
138 |
10 |
p. 1183-1200
|
artikel
|
| 8 |
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3
|
Xiao, Xueshan
|
|
2019
|
138 |
10 |
p. 1077-1090
|
artikel
|
| 9 |
Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish
|
Waksmunski, Andrea R.
|
|
2019
|
138 |
10 |
p. 1171-1182
|
artikel
|
| 10 |
Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic histories
|
Ceballos, Francisco C.
|
|
2019
|
138 |
10 |
p. 1123-1142
|
artikel
|
| 11 |
The rare 13q33–q34 microdeletions: eight new patients and review of the literature
|
Sagi-Dain, Lena
|
|
2019
|
138 |
10 |
p. 1145-1153
|
artikel
|
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