Holoprosencephaly in deletions of proximal chromosome 14q [1]

Journal of Medical Genetics

Volumn 35, Issue 7, 1998, Pages 612-

  Devriendt, K ^a   Fryns, J P ^a   Chen, C P ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN;

CHROMOSOME 14Q; CHROMOSOME DELETION; COSMID; DIENCEPHALON; ENVIRONMENTAL FACTOR; GENE DELETION; GENE MAPPING; HOLOPROSENCEPHALY; HUMAN; LETTER; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 14; HOLOPROSENCEPHALY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICE; MICE, KNOCKOUT; NUCLEAR PROTEINS; PHENOTYPE; TRANSCRIPTION FACTORS;

EID: 0031840928     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (11)