Literature DB >> 11303516

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

F K Wong, H Koillinen, J Rautio, B T Teh, R Ranta, A Karsten, O Larson, S Linder-Aronson, J Huggare, C Larsson, J Kere.   

Abstract

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Year:  2001        PMID： 11303516      PMCID： PMC1734824          DOI： 10.1136/jmg.38.3.198

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  2 in total

Review 1.  Developmental disorders of the dentition: an update.

Authors:  Ophir D Klein; Snehlata Oberoi; Ann Huysseune; Maria Hovorakova; Miroslav Peterka; Renata Peterkova
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

2.  Monozygotic twins with variable expression of Van der Woude syndrome.

Authors:  Rebekah Jobling; Raechel A Ferrier; Ross McLeod; Aline Lourenco Petrin; Jeffrey C Murray; Mary Ann Thomas
Journal:  Am J Med Genet A       Date:  2011-07-07       Impact factor: 2.802
  2 in total

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