Hirschsprung disease and L1CAM: is the disturbed sex ratio caused by L1CAM mutations?

Journal of medical genetics

Volumn 39, Issue 3, 2002, Pages

  Hofstra, R M ^a   Elfferich, P ^a   Osinga, J ^a   Verlind, E ^a   Fransen, E ^a   Lopez Pison J ^a   de Die Smulders, C E ^a   Stolte Dijkstra, I ^a   Buys, C H ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALGRANULIN; MEMBRANE PROTEIN; NERVE CELL ADHESION MOLECULE;

CHILD; EXON; FEMALE; GENETIC VARIABILITY; GENETICS; HIRSCHSPRUNG DISEASE; HUMAN; LETTER; MALE; MUTATION; NEWBORN; NUCLEOTIDE SEQUENCE; RNA SPLICING; SEX RATIO;

BASE SEQUENCE; CHILD; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HIRSCHSPRUNG DISEASE; HUMANS; INFANT, NEWBORN; LEUKOCYTE L1 ANTIGEN COMPLEX; MALE; MEMBRANE GLYCOPROTEINS; MUTATION; NEURAL CELL ADHESION MOLECULES; RNA SPLICE SITES; SEX DISTRIBUTION; SEX RATIO; VARIATION (GENETICS);

MLCS; MLOWN;

EID: 17944401148     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.39.3.e11     Document Type: Letter

References (0)