Spontaneous evolution of an unusual cortical malformation in SOX2 anophthalmia syndrome.

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Spontaneous evolution of an unusual cortical malformation in SOX2 anophthalmia syndrome.

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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Spontaneous evolution of an unusual cortical malformation in SOX2 anophthalmia syndrome.

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Spontaneous evolution of an unusual cortical malformation in SOX2 anophthalmia syndrome.

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Spontaneous evolution of an unusual cortical malformation in SOX2 anophthalmia syndrome.

@en

P1476

Spontaneous evolution of an unusual cortical malformation in SOX2 anophthalmia syndrome.

@en

P2093

Jay Desai

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Tena Rosser

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P2860

A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2

SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development

Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans

Mutations in SOX2 cause anophthalmia.

Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome.

SOX genes and neural progenitor identity.

SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions.

From stem cells to neurons and glia: a Soxist's view of neural development.

The role of SOX2 in hypogonadotropic hypogonadism.

P304

422-424

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P31

scholarly article

case report

P356

10.4103/0972-2327.116924

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P433

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P478

http://www.w3.org/2001/XMLSchema#string

P577

2013-07-01T00:00:00Z

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P698

24101835

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P932

3788299

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