A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly.

scientific article published in July 2004

A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/AJMG.A.30070
P698PubMed publication ID15213999
P5875ResearchGate publication ID8494238

P2093author name stringMauricio R Delgado
Elaine E Stashinko
Jin S Hahn
Eric B Levey
Nancy J Clegg
Heather A Kammann
Vicki T Sweet
P2860cites workNeuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brainQ40628479
Cytogenetic variants in holoprosencephaly. Report of a case and review of the literatureQ41674387
Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtypeQ48420222
Genetic epidemiology and congenital malformations: from the chromosome to the cribQ77868245
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectholoprosencephalyQ1459821
P304page(s)114-119
P577publication date2004-07-01
P1433published inAmerican Journal of Medical GeneticsQ4744254
P1476titleA retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly.
P478volume128A

Reverse relations

cites work (P2860)
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Q38029000Fatally flawed? A review and ethical analysis of lethal congenital malformations
Q28973601Hedgehog signaling promotes basal progenitor expansion and the growth and folding of the neocortex
Q31097430Holoprosencephaly
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Q38696737Holoprosencephaly: antenatal and postnatal diagnosis and outcome
Q35973166Links between abnormal brain structure and cognition in holoprosencephaly
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Q87484006Neonatal outcomes of fetuses diagnosed with life-limiting conditions when individualized comfort measures are proposed
Q41789254Non-visualisation of cavum septi pellucidi: implication in prenatal diagnosis?
Q34325586PTCH1 duplication in a family with microcephaly and mild developmental delay
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Q42968879Prenatal-postnatal correlations of brain abnormalities: how lesions and diagnoses change over time
Q48494005Rare Disease: Lobar Holoprosencephaly With a Median Cleft Lip-Case Report
Q35546457TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype