Page last updated: 2024-08-26

nsc-172755 and Anemia, Hemolytic, Congenital

nsc-172755 has been researched along with Anemia, Hemolytic, Congenital in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	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
Dhermy, D; Fournier, CM; Gallagher, PG; Grandchamp, B; Lecomte, MC; Nicolas, G	1

Other Studies

1 other study(ies) available for nsc-172755 and Anemia, Hemolytic, Congenital

Article	Year
Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemia. Blood, 1997, Jun-15, Volume: 89, Issue:12 Topics: Adult; Alleles; Anemia, Hemolytic, Congenital; Benin; Black People; DNA, Complementary; Erythrocytes, Abnormal; Exons; France; Gene Frequency; Genotype; Guadeloupe; Humans; Infant, Newborn; Male; Mutagenesis, Insertional; Mutation; Open Reading Frames; RNA Splicing; RNA, Messenger; Spectrin	1997

Article

Year

Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemia.

Blood, 1997, Jun-15, Volume: 89, Issue:12

Topics: Adult; Alleles; Anemia, Hemolytic, Congenital; Benin; Black People; DNA, Complementary; Erythrocytes, Abnormal; Exons; France; Gene Frequency; Genotype; Guadeloupe; Humans; Infant, Newborn; Male; Mutagenesis, Insertional; Mutation; Open Reading Frames; RNA Splicing; RNA, Messenger; Spectrin

1997