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Microcephaly with or Without Chorioretinopathy, Lymphoedema, or Mental Retardation (Mclmr): Review of Phenotype Associated with Kif11 Mutations
AuthID
P-009-J6M
P-009-J6M
21
Author(s)
Jones, GE
·Ostergaard, P
·Moore, AT
·Connell, FC
·Williams, D
·Brady, AF
·Spier, I
·Moldovan, O
·[+1]·
Mikat, B
·Coubes, C
·Saul, RA
·Brice, G
·Jeffery, S
·Mortimer, PS
·Vasudevan, PC
·Mansour, S
Document Type
Article
Year published
2014
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 22, Issue: 7, Pages: 881-887 (7)
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ISSN: 1018-4813
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Name Order | Name | Name Order | Name | Name Order | Name | ||
---|---|---|---|---|---|---|---|
1 | Jones, GE; | 2 | Ostergaard, P; | 3 | Moore, AT; | ||
4 | Connell, FC; | 5 | Williams, D; | 6 | Quarrell, O; | ||
7 | Brady, AF; | 8 | Spier, I; | 9 | Hazan, F; | ||
10 | Moldovan, O; | 11 | Wieczorek, D; | 12 | Mikat, B; | ||
13 | Petit, F; | 14 | Coubes, C; | 15 | Saul, RA; | ||
16 | Brice, G; | 17 | Gordon, K; | 18 | Jeffery, S; | ||
19 | Mortimer, PS; | 20 | Vasudevan, PC; | 21 | Mansour, S; |