Terminal 2q deletion--a recognizable syndrome.

Clinical genetics

Volumn 51, Issue 4, 1997, Pages 290-

  Wenger, S L ^a   Boone, L Y ^a   Surti, U ^a   Steele, M W ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 2; CHROMOSOME DELETION; GENETICS; HUMAN; MULTIPLE MALFORMATION SYNDROME; NEWBORN; NOTE; SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 2; HUMANS; INFANT, NEWBORN; SYNDROME;

MLCS; MLOWN;

EID: 0031113937     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02475.x     Document Type: Note

References (0)