Prenatal detection of Fanconi anemia

Indian Pediatrics

Volumn 51, Issue 6, 2014, Pages 501-

  Solanki, Avani ^a   Vundinti, Babu Rao ^a  

^a NATIONAL INSTITUTE OF IMMUNOHAEMATOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

FANCONI ANEMIA GROUP A PROTEIN; FANCONI ANEMIA GROUP D2 PROTEIN; GENOMIC DNA; MITOMYCIN; FANCA PROTEIN, HUMAN;

AMNION CELL; APLASTIC ANEMIA; CASE REPORT; CELL CULTURE; CHILD; CHORION VILLUS; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; FANCONI ANEMIA; FEMALE; FETUS; GENE MUTATION; GESTATIONAL AGE; HETEROZYGOSITY; HETEROZYGOTE; HUMAN; HUMAN TISSUE; LETTER; MUTATIONAL ANALYSIS; PRENATAL DIAGNOSIS; PRESCHOOL CHILD; WESTERN BLOTTING; CHORION VILLUS SAMPLING; FATHER; GENETICS; MALE; MOTHER; NUCLEOTIDE SEQUENCE; PREGNANCY; PROCEDURES;

ANEMIA, APLASTIC; CHILD, PRESCHOOL; CHORIONIC VILLI SAMPLING; CHROMOSOME BREAKAGE; DNA MUTATIONAL ANALYSIS; FANCONI ANEMIA; FANCONI ANEMIA COMPLEMENTATION GROUP A PROTEIN; FATHERS; FEMALE; HUMANS; MALE; MOTHERS; PREGNANCY;

EID: 84905126570     PISSN: 00196061     EISSN: 09747559     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)

1. Gillio AP, Verlander PC, Batish SD, Giampietro PF, Auerbach AD. Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an international Fanconi anemia registry study. Blood. 1997;90:105-10. (Pubitemid 27276553)
2. GraciaHiguera I, Taniguchi T, Ganesan S, Meyn MS, Timmers C, Hejna J, et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol Cell. 2001;7:249-62.
3. deWinter JP, Joenje H. The genetic and molecular basis of Fanconi anemia. Mutation Research. 2009;668:11-9.
4. Vaz F, Hanenberg H, Schuster B, Barker K, Wiek C, Erven V, et al. Mutation of the RAD51C gene in a Fanconi anemia-like disorder. Nature Gene. 2010;42:406-9.