(Q41724098)

8 October 2017

title

Holoprosencephaly: molecular study of a California population (English)

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8 October 2017

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1 reference

Nanni L

1

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8 October 2017

Croen LA

series ordinal

2

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8 October 2017

Lammer EJ

series ordinal

3

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8 October 2017

Muenke M

series ordinal

4

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8 October 2017

publication date

1 February 2000

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American Journal of Medical Genetics Part A

8 October 2017

published in

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8 October 2017

volume

90

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8 October 2017

issue

4

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8 October 2017

page(s)

315-319

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Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

8 October 2017

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A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif

21 January 2018

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Expression of a novel murine homeobox gene in the developing cerebellar external granular layer during its proliferation.

21 January 2018

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mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America?

21 January 2018

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Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

21 January 2018

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The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system

21 January 2018

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Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

21 January 2018

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Birth defects monitoring in California: a resource for epidemiological research

21 January 2018

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Holoprosencephaly: epidemiologic and clinical characteristics of a California population

21 January 2018

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Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity

21 January 2018

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Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

21 January 2018

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Retinoic acid embryopathy

21 January 2018

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Six3 overexpression initiates the formation of ectopic retina

21 January 2018

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Biochemical evidence that patched is the Hedgehog receptor

21 January 2018

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Holoprosencephaly in human embryos: Epidemiologic studies of 150 cases

21 January 2018

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Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity

21 January 2018

1 reference

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A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

21 January 2018

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The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation

21 January 2018

1 reference

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The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.

21 January 2018

1 reference

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Ectopic lens induction in fish in response to the murine homeobox gene Six3.

21 January 2018

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Floor plate and motor neuron induction by vhh-1, a vertebrate homolog of hedgehog expressed by the notochord

21 January 2018

1 reference

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Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

21 January 2018

1 reference

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Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly

21 January 2018

1 reference

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Holoprosencephaly: a paradigm for the complex genetics of brain development

21 January 2018

1 reference

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Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.

21 January 2018

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Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly

21 January 2018

1 reference

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Molecular mechanisms of holoprosencephaly

21 January 2018

1 reference

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Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

21 January 2018

1 reference

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A Smad transcriptional corepressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000214%2990%3A4%3C315%3A%3AAID-AJMG10%3E3.0.CO%3B2-Y

10.1002/(SICI)1096-8628(20000214)90:4<315::AID-AJMG10>3.0.CO;2-Y

21 January 2018

Identifiers

DOI

1 reference

8 October 2017

1 reference