cysteine and Facies

cysteine has been researched along with Facies in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bonaventure, J; El Ghouzzi, V; Heuertz, S; Lajeunie, E; Le Merrer, M; Martinovic, J; Renier, D	1

Other Studies

1 other study(ies) available for cysteine and Facies

Article	Year
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome. European journal of human genetics : EJHG, 2006, Volume: 14, Issue:3 Topics: Acrocephalosyndactylia; Codon, Terminator; Cohort Studies; Craniosynostoses; Cysteine; DNA Mutational Analysis; Exons; Facies; Genotype; Heterozygote; Homozygote; Humans; Mutation; Mutation, Missense; Phenotype; Prognosis; Protein Isoforms; Receptor, Fibroblast Growth Factor, Type 1; Receptor, Fibroblast Growth Factor, Type 2; Receptor, Fibroblast Growth Factor, Type 3; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA	2006

Article

Year

Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome.

European journal of human genetics : EJHG, 2006, Volume: 14, Issue:3

Topics: Acrocephalosyndactylia; Codon, Terminator; Cohort Studies; Craniosynostoses; Cysteine; DNA Mutational Analysis; Exons; Facies; Genotype; Heterozygote; Homozygote; Humans; Mutation; Mutation, Missense; Phenotype; Prognosis; Protein Isoforms; Receptor, Fibroblast Growth Factor, Type 1; Receptor, Fibroblast Growth Factor, Type 2; Receptor, Fibroblast Growth Factor, Type 3; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA

2006