Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: Contradictory results (multiple letters)

American Journal of Human Genetics

Volumn 77, Issue 5, 2005, Pages 892-894

  Castiglia, L ^a   Fichera, Marco ^a   Romano, C ^a   Galesi, O ^a   Grillo, L ^a   Sturnio, M ^a   Failla, P ^a   Klaassens, M ^b   Tibboel, D ^b   Oostra, B A ^b   De Klein, Annnelies ^b  

^a OASI RESEARCH INSTITUTE IRCCS   (Italy)

^b ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

NERVE CELL ADHESION MOLECULE;

ADOLESCENT; CASE REPORT; CHROMOSOME 15P; CHROMOSOME ABERRATION; CONGENITAL DIAPHRAGM HERNIA; DIAPHRAGM HERNIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE EXPRESSION; GENE LOCUS; HUMAN; LETTER; MENTAL RETARDATION MALFORMATION SYNDROME; NR2F2 GENE; PRIORITY JOURNAL; ST8SIA2 GENE;

EID: 27244434036     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/497082     Document Type: Letter

References (10)

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