Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature.

Journal of medical genetics.

Volumn 43, Issue 2, 2006, Pages

  Mensink, K A ^a   Ketterling, R P ^a   Flynn, H C ^a   Knudson, R A ^a   Lindor, N M ^a   Heese, B A ^a   Spinner, R J ^a   Babovic Vuksanovic, D ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

NEUROFIBROMIN;

ADOLESCENT; ADULT; CASE REPORT; CHILD; CONNECTIVE TISSUE DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETICS; HUMAN; INFANT; LETTER; MALE; NEOPLASM; PHENOTYPE; PRESCHOOL CHILD; REPRODUCIBILITY;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CONNECTIVE TISSUE DISEASES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; NEOPLASMS; NEUROFIBROMIN 1; PHENOTYPE; REPRODUCIBILITY OF RESULTS; SEQUENCE DELETION;

EID: 33746934199     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: None     Document Type: Letter

References (39)