proline and Synostosis

proline has been researched along with Synostosis in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baten, E; Debeer, P; Devriendt, K; Fryns, JP; Huysmans, C; Van de Ven, WJ	1
Büsse-Ratzka, M; Collmann, H; Hoppe, F; Krauss, J; Kress, W; Kunz, J; Lieb, G; Pahnke, J; Petersen, B; Reinhart, E; Schäfer, WD; Schropp, C; Sold, J; Sörensen, N; Trusen, A	1

Other Studies

2 other study(ies) available for proline and Synostosis

Article	Year
A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostoses. American journal of medical genetics. Part A, 2004, Aug-01, Volume: 128A, Issue:4 Topics: Abnormalities, Multiple; Arginine; Base Sequence; Bone Morphogenetic Proteins; Carpal Bones; Carrier Proteins; Mutation; Proline; Radiography; Synostosis; Tarsal Bones	2004
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome. European journal of human genetics : EJHG, 2006, Volume: 14, Issue:1 Topics: Acrocephalosyndactylia; Adolescent; Amino Acid Substitution; Arginine; Child, Preschool; Ear; Hearing Loss, Sensorineural; Humans; Intellectual Disability; Intracranial Pressure; Mutation; Nuclear Proteins; Pedigree; Proline; Receptor, Fibroblast Growth Factor, Type 3; Repetitive Sequences, Nucleic Acid; Syndrome; Synostosis; Twist-Related Protein 1	2006

Article

Year

A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostoses.

American journal of medical genetics. Part A, 2004, Aug-01, Volume: 128A, Issue:4

Topics: Abnormalities, Multiple; Arginine; Base Sequence; Bone Morphogenetic Proteins; Carpal Bones; Carrier Proteins; Mutation; Proline; Radiography; Synostosis; Tarsal Bones

2004

Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.

European journal of human genetics : EJHG, 2006, Volume: 14, Issue:1

Topics: Acrocephalosyndactylia; Adolescent; Amino Acid Substitution; Arginine; Child, Preschool; Ear; Hearing Loss, Sensorineural; Humans; Intellectual Disability; Intracranial Pressure; Mutation; Nuclear Proteins; Pedigree; Proline; Receptor, Fibroblast Growth Factor, Type 3; Repetitive Sequences, Nucleic Acid; Syndrome; Synostosis; Twist-Related Protein 1

2006