| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A lethal phenotype associated with tissue plasminogen deficiency in humans
|
Shamseldin, Hanan E.
|
|
2016
|
135 |
10 |
p. 1209-1211
|
artikel
|
| 2 |
CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly
|
Basit, Sulman
|
|
2016
|
135 |
10 |
p. 1199-1207
|
artikel
|
| 3 |
Genetic alterations of δ-catenin/NPRAP/Neurojungin (CTNND2): functional implications in complex human diseases
|
Lu, Qun
|
|
2016
|
135 |
10 |
p. 1107-1116
|
artikel
|
| 4 |
Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry
|
Qian, Frank
|
|
2016
|
135 |
10 |
p. 1145-1159
|
artikel
|
| 5 |
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2
|
Henden, Lyndal
|
|
2016
|
135 |
10 |
p. 1117-1125
|
artikel
|
| 6 |
Immunoglobulin G genotypes and the risk of schizophrenia
|
Pandey, Janardan P.
|
|
2016
|
135 |
10 |
p. 1175-1179
|
artikel
|
| 7 |
Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans
|
Shaheen, Ranad
|
|
2016
|
135 |
10 |
p. 1191-1197
|
artikel
|
| 8 |
Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith–Magenis syndrome with evident peripheral neuropathy
|
Yuan, Bo
|
|
2016
|
135 |
10 |
p. 1161-1174
|
artikel
|
| 9 |
The genetic history of Cochin Jews from India
|
Waldman, Yedael Y.
|
|
2016
|
135 |
10 |
p. 1127-1143
|
artikel
|
| 10 |
Three novel missense mutations in the filamin B gene are associated with isolated congenital talipes equinovarus
|
Yang, Haiou
|
|
2016
|
135 |
10 |
p. 1181-1189
|
artikel
|
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