arginine and Brachydactylia

arginine has been researched along with Brachydactylia 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	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Birnbaum, R; Gur, H; Kidron, D; Lerman-Sagie, T; Lev, D; Malinger, G; Yanoov-Sharav, M; Yosha-Orpaz, N; Yosovich, K	1
Blaser, S; Boycott, KM; Chitayat, D; Dyment, DA; Kernohan, KD; Majewski, J; Martin, N; McBride, A; Schwartzentruber, J; Xi, Y	1

Other Studies

2 other study(ies) available for arginine and Brachydactylia

Article	Year
Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations. American journal of medical genetics. Part A, 2019, Volume: 179, Issue:1 Topics: Arginine; Astrocytoma; Brachydactyly; Developmental Disabilities; Female; Fetal Growth Retardation; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Methylation; Muscle Hypotonia; Mutation; Orbital Neoplasms; Pregnancy; Protein-Arginine N-Methyltransferases	2019
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly. Clinical genetics, 2017, Volume: 91, Issue:5 Topics: Abnormalities, Multiple; Arginine; Brachydactyly; Child, Preschool; Chromosomes, Human, Pair 16; Face; Female; Fingers; Gene Deletion; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Microcephaly; Protein-Arginine N-Methyltransferases; Transcription Initiation Site; Wnt Signaling Pathway	2017

Article

Year

Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations.

American journal of medical genetics. Part A, 2019, Volume: 179, Issue:1

Topics: Arginine; Astrocytoma; Brachydactyly; Developmental Disabilities; Female; Fetal Growth Retardation; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Methylation; Muscle Hypotonia; Mutation; Orbital Neoplasms; Pregnancy; Protein-Arginine N-Methyltransferases

2019

Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly.

Clinical genetics, 2017, Volume: 91, Issue:5

Topics: Abnormalities, Multiple; Arginine; Brachydactyly; Child, Preschool; Chromosomes, Human, Pair 16; Face; Female; Fingers; Gene Deletion; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Microcephaly; Protein-Arginine N-Methyltransferases; Transcription Initiation Site; Wnt Signaling Pathway

2017