phenylalanine and Labhart-Willi Syndrome

phenylalanine has been researched along with Labhart-Willi Syndrome in 1 studies

Research

Studies (1)

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

Authors

Authors	Studies
Butler, MG	1

Other Studies

1 other study(ies) available for phenylalanine and Labhart-Willi Syndrome

Article	Year
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome. American journal of human genetics, 1989, Volume: 45, Issue:1 Topics: Adolescent; Adult; Catecholamines; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 15; Eye Color; Female; Hair Color; Humans; Infant; Male; Melanocyte-Stimulating Hormones; Phenylalanine; Pigmentation Disorders; Prader-Willi Syndrome; Skin; Tyrosine	1989

Article

Year

Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

American journal of human genetics, 1989, Volume: 45, Issue:1

Topics: Adolescent; Adult; Catecholamines; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 15; Eye Color; Female; Hair Color; Humans; Infant; Male; Melanocyte-Stimulating Hormones; Phenylalanine; Pigmentation Disorders; Prader-Willi Syndrome; Skin; Tyrosine

1989