Strømme Syndrome Is a Ciliary Disorder Caused by Mutations inCENPF

The kinetochore protein,CENPF, is mutated in human ciliopathy and microcephaly phenotypes

(2015) Aoife M Waters et al.   JOURNAL OF MEDICAL GENETICS

Whole exome sequence analysis of Peters anomaly

(2014) Eric Weh et al.   HUMAN GENETICS

Cardiac-specific deletion of the microtubule-binding protein CENP-F causes dilated cardiomyopathy

(2012) E. Dees et al.   Disease Models & Mechanisms

Apple peel intestinal atresia in siblings with ocular anomalies and microcephaly

(2010) Petter Strømme et al.   CLINICAL GENETICS

Further evidence for a syndrome of “apple peel” intestinal atresia, ocular anomalies and microcephaly

(2010) Jennie Slee et al.   CLINICAL GENETICS

Developmental aspects in apple peel intestinal atresia - ocular anomalies - microcephaly syndrome

(2010) Petter Strømme et al.   CLINICAL GENETICS

CEP290, a gene with many faces: mutation overview and presentation of CEP290base

(2010) Frauke Coppieters et al.   HUMAN MUTATION

Cdc20 is required for the post-anaphase, KEN-dependent degradation of centromere protein F

(2010) M. D. J. Gurden et al.   JOURNAL OF CELL SCIENCE

United States Head Circumference Growth Reference Charts: Birth to 21 Years

(2010) Jonathan D. Rollins et al.   JOURNAL OF PEDIATRICS

Silencing CENPF in bovine preimplantation embryo induces arrest at 8-cell stage

(2009) Tereza Toralová et al.   REPRODUCTION

Exclusion of aPAX6,FOXC1,PITX2, andMYCN mutation in another patient with apple peel intestinal atresia, ocular anomalies and microcephaly and review of the literature

(2008) Yolande van Bever et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A