A 223-kb de novo deletion of pax9 in a patient with oligodontia

Journal of Craniofacial Surgery

Volumn 21, Issue 3, 2010, Pages 837-839

  Haldeman Englert, Chad R ^a,b   Biser, Alisha ^a   Zackai, Elaine H ^a,c   Ming, Jeffrey E ^a,c  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b WAKE FOREST SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Microarray; Microdeletion; Oligodontia; PAX9

Indexed keywords

TRANSCRIPTION FACTOR PAX9;

CASE REPORT; CONFERENCE PAPER; GENE DELETION; GENETICS; HUMAN; HYPODONTIA; KLINEFELTER SYNDROME; LANGUAGE DISABILITY; MALE; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

ANODONTIA; CHILD, PRESCHOOL; HUMANS; KLINEFELTER SYNDROME; LANGUAGE DISORDERS; MALE; PAX9 TRANSCRIPTION FACTOR; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE DELETION;

EID: 77952793045     PISSN: 10492275     EISSN: None     Source Type: Journal    
DOI: 10.1097/SCS.0b013e3181d87912     Document Type: Conference Paper

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