phenylalanine and Disomy, Uniparental

phenylalanine has been researched along with Disomy, Uniparental in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aboura, A; Capel, L; Gajdos, V; Labrune, P; Lachaux, A; Parisot, F; Petit, FM; Poüs, C; Tachdjian, G1

Other Studies

1 other study(ies) available for phenylalanine and Disomy, Uniparental

ArticleYear
Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.
    European journal of human genetics : EJHG, 2005, Volume: 13, Issue:3

    Topics: Base Sequence; Bilirubin; Chromosome Mapping; Chromosomes, Human, Pair 2; Crigler-Najjar Syndrome; DNA; Fatal Outcome; Fathers; Glucuronosyltransferase; Humans; Infant; Infant, Newborn; Male; Microsatellite Repeats; Mothers; Phenylalanine; Sequence Deletion; Uniparental Disomy

2005