Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia.

Journal of medical genetics

Volumn 41, Issue 5, 2004, Pages

  Wieland, I ^a   Muschke, P ^a   Jakubiczka, S ^a   Volleth, M ^a   Freigang, B ^a   Wieacker, P F ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

CASE REPORT; CHROMOSOME 7; CHROMOSOME DELETION; CONGENITAL MALFORMATION; FOOT MALFORMATION; GENETICS; GENOTYPE; HAND MALFORMATION; HEARING IMPAIRMENT; HUMAN; INNER EAR; LETTER; MALE; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PERCEPTION DEAFNESS; PRESCHOOL CHILD;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; DEAFNESS; EAR, INNER; FOOT DEFORMITIES, CONGENITAL; GENOTYPE; HAND DEFORMITIES, CONGENITAL; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MICROSATELLITE REPEATS;

EID: 3042764746     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2003.010587     Document Type: Letter

References (0)