Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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Developmental disorders of the dentition: an update.Alobar Holoprosencephaly Associated with Meningomyelocoele and Omphalocoele: An Unusual Coexistence Rare Disease: Lobar Holoprosencephaly With a Median Cleft Lip-Case Report.

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Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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P1476

Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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P2093

Francesca Lami

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Monica Marini

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Paola Ferrari

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Viola Alesi

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P2860

Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations

Holoprosencephaly.

De novo 7q36 deletion: breakpoint analysis and types of holoprosencephaly.

Analysis of genotype-phenotype correlations in human holoprosencephaly.

Autosomal dominant sacral agenesis: Currarino syndrome.

New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Idiopathic syringomyelia: retrospective case series, comprehensive review, and update on management.

The product of hedgehog autoproteolytic cleavage active in local and long-range signalling.

Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog.

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s12041-013-0215-5

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97-101

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scholarly article

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10.1007/S12041-013-0215-5

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P433

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P478

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Diana Carli

Lorenzo Iughetti

Antonio Percesepe

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2013-04-01T00:00:00Z

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23640411

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P921

holoprosencephaly

Holoprosencephaly: report of four cases and genotype-phenotype correlations.

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P2860

P2860

Holoprosencephaly: report of four cases and genotype-phenotype correlations.

description

name

type

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prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P921

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P1433

P1476

P2093

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P2888

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P356

P433

P478

P50

P577

P698

P921