Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking

By Hsiao Yi-Chun   Tong Zachary J.   Westfall Jennifer E.   Ault Jeffrey G.   Page-McCaw Patrick S.   Ferland Russell J.  

Human Molecular Genetics, Vol. 18, Iss. 20, 2009-10 ,pp. : 3926-3941

Oxford University Press

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Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

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Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 373-380

Oxford University Press

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Association of variants in the PCSK1 gene with obesity in the EPIC-Norfolk study

By Kilpelinen Tuomas O.   Bingham Sheila A.   Khaw Kay-Tee   Wareham Nicholas J.   Loos Ruth J.F.  

Human Molecular Genetics, Vol. 18, Iss. 18, 2009-09 ,pp. : 3496-3501

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An association between variants in the IGF2 gene and Beckwith–Wiedemann syndrome: interaction between genotype and epigenotype

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A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome

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Public Health Genomics, Vol. 20, Iss. 3, 2017-07 ,pp. : 188-193

Karger

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