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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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J Rautio

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Clinical Genetics|July 31, 2007

Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palateA M Koivisto, S Ala-Mello, S Lemmelä, et al.

Epigenetics|March 21, 2012

Neonatal MeCP2 is important for the organization of sex differences in vasopressin expressionRobin M Forbes-Lorman, Jared J Rautio, Joseph R Kurian, et al.

European Journal of Human Genetics : EJHG|January 10, 2002

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34H Koillinen, F K Wong, J Rautio, et al.

Journal of Medical Genetics|May 19, 2001

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndromeF K Wong, H Koillinen, J Rautio, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

Clinical Genetics|July 31, 2007

Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palateA M Koivisto, S Ala-Mello, S Lemmelä, et al.

Epigenetics|March 21, 2012

Neonatal MeCP2 is important for the organization of sex differences in vasopressin expressionRobin M Forbes-Lorman, Jared J Rautio, Joseph R Kurian, et al.

European Journal of Human Genetics : EJHG|January 10, 2002

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34H Koillinen, F K Wong, J Rautio, et al.

Journal of Medical Genetics|May 19, 2001

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndromeF K Wong, H Koillinen, J Rautio, et al.

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