Exclusion of 22q11 deletion in Noonan syndrome with tetralogy of Fallot.

American journal of medical genetics

Volumn 62, Issue 4, 1996, Pages 413-414

  Digilio, M C ^a   Marino, B ^a   Giannotti, A ^a   Dallapiccola, B ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHILD; CHROMOSOME 22; CHROMOSOME DELETION; FALLOT TETRALOGY; FEMALE; GENETICS; HUMAN; INFANT; MALE; NOONAN SYNDROME; NOTE;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; INFANT; MALE; NOONAN SYNDROME; TETRALOGY OF FALLOT;

EID: 0030599863     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320620404     Document Type: Note

References (0)