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J Martinovic

Showing results (41-50 of 46) with videos related to

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Clinical Oral Investigations|July 10, 2020
Re-focusing on Agnathia-Otocephaly complexC Dubucs, N Chassaing, C Sergi, et al.
European Journal of Medical Genetics|February 4, 2014
SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplicationA Briand-Suleau, J Martinovic, L Tosca, et al.
Journal of Medical Genetics|September 20, 2005
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human developmentD Sanlaville, H C Etchevers, M Gonzales, et al.
Clinical Genetics|December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndromeM Nizon, M Henry, C Michot, et al.
Human Mutation|June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephalyC Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Kidney International|November 27, 2009
Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney diseaseErick Denamur, Anne-Lise Delezoide, Corinne Alberti, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Clinical Oral Investigations|July 10, 2020
Re-focusing on Agnathia-Otocephaly complexC Dubucs, N Chassaing, C Sergi, et al.
European Journal of Medical Genetics|February 4, 2014
SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplicationA Briand-Suleau, J Martinovic, L Tosca, et al.
Journal of Medical Genetics|September 20, 2005
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human developmentD Sanlaville, H C Etchevers, M Gonzales, et al.
Clinical Genetics|December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndromeM Nizon, M Henry, C Michot, et al.
Human Mutation|June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephalyC Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Kidney International|November 27, 2009
Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney diseaseErick Denamur, Anne-Lise Delezoide, Corinne Alberti, et al.
Pageof 5