Page last updated: 2024-08-26

nsc-172755 and Skin Abnormalities

nsc-172755 has been researched along with Skin Abnormalities 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	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abramovicz, M; Alao, MJ; Arveiler, B; Hans, Ch; Lacombe, D; Lalèyè, A; Lalya, F; Morice-Picard, F; Rooryck, C	1

Other Studies

1 other study(ies) available for nsc-172755 and Skin Abnormalities

Article	Year
Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African female. European journal of medical genetics, 2012, Volume: 55, Issue:11 Topics: Benin; Black People; Blepharophimosis; Chromosome Deletion; Chromosomes, Human, Pair 3; Female; Forkhead Box Protein L2; Forkhead Transcription Factors; Humans; Infant; Menopause, Premature; Skin Abnormalities; Translocation, Genetic	2012

Article

Year

Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African female.

European journal of medical genetics, 2012, Volume: 55, Issue:11

Topics: Benin; Black People; Blepharophimosis; Chromosome Deletion; Chromosomes, Human, Pair 3; Female; Forkhead Box Protein L2; Forkhead Transcription Factors; Humans; Infant; Menopause, Premature; Skin Abnormalities; Translocation, Genetic

2012