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Holoprosencephaly: Report of four cases and genotype-phenotype correlations

By F. Lami, D. Carli, P. Ferrari, M. Marini, V. Alesi, L. Iughetti and A. Percesepe
Topics: 7q36 deletion; Currarino syndrome; holoprosencephaly; SHH gene mutation; Abortion, Eugenic; Chromosomes, Human, Pair 7; Comparative Genomic Hybridization; Female; Genetic Association Studies; Hedgehog Proteins; Holoprosencephaly; Humans; Infant, Newborn; Male; Sequence Deletion; Ultrasonography, Prenatal
Publisher: 'Springer Science and Business Media LLC'
Year: 2013
DOI identifier: 10.1007/s12041-013-0215-5
OAI identifier: oai:iris.unito.it:2318/1742178

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