Unusual variant of holoprosencephaly in monosomy 13q

Pediatric and Developmental Pathology

Volumn 5, Issue 2, 2002, Pages 170-178

  Marcorelles, Pascale ^a   Loget, Philippe ^b   Fallet Bianco, Catherine ^c   Roume, Joëlle ^d   Encha Razavi, Ferechte ^e   Delezoide, Anne Lise ^f  

^a CHU MORVAN   (France)

^b Cabinet d'Anatomie et Cytologie Pathologiques Richier   (France)

^c CENTRE HOSPITALIER SAINTE ANNE   (France)

^d HÔPITAL SAINT ANTOINE   (France)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

^f HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

Cerebral midline anomalies; Holoprosencephaly; Monosomy 13; ZIC

Indexed keywords

ARTICLE; CHROMOSOME 13Q; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CYTOGENETICS; FEMALE; FETUS; FETUS ECHOGRAPHY; GENE LOSS; GENE MUTATION; HOLOPROSENCEPHALY; HUMAN; HUMAN CELL; MALE; MONOSOMY; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPIC VARIATION; PRIORITY JOURNAL;

ADULT; CEREBRAL CORTEX; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; FEMALE; HOLOPROSENCEPHALY; HUMANS; MALE; PREGNANCY; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0036244763     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10024001-0200-5     Document Type: Article

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