Unusual variant of holoprosencephaly in monosomy 13q.

Marcorelles, Pascale

Unusual variant of holoprosencephaly in monosomy 13q. [electronic resource] - Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society - 170-8 p. digital

Publication Type: Case Reports; Journal Article

1093-5266

10.1007/s10024001-0200-5 doi


Adult
Cerebral Cortex--abnormalities
Chromosome Deletion
Chromosomes, Human, Pair 13
Female
Holoprosencephaly--genetics
Humans
Male
Nuclear Proteins
Pregnancy
Syndrome
Transcription Factors--genetics