Holoprosencephaly: a guide to diagnosis and clinical management - Test2 - elhamkhani - TriplyDB

Holoprosencephaly: a guide to diagnosis and clinical management

Holoprosencephaly: a guide to diagnosis and clinical management

http://www.wikidata.org/entity/Q34041428

about

The human brain and face: mechanisms of cranial, neurological and facial development revealed through malformations of holoprosencephaly, cyclopia and aberrations in chromosome 18 Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs Love and the Value of Life in Health Care: A Narrative Medicine Case Study in Medical Education Semilobar holoprosencephaly with 21q22 deletion: an autopsy report.Diffusion tensor imaging and fiber tractography in brain malformations.Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies.Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review MRI of lobar holoprosencephaly in a cat with hypodipsic hypernatraemia

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Holoprosencephaly: a guide to diagnosis and clinical management

http://www.wikidata.org/entity/Q34041428

description

2011 nî lūn-bûn

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2011 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2011 թվականի հունիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Holoprosencephaly: a guide to diagnosis and clinical management

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Holoprosencephaly: a guide to diagnosis and clinical management

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Holoprosencephaly: a guide to diagnosis and clinical management

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Holoprosencephaly: a guide to diagnosis and clinical management

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Holoprosencephaly: a guide to diagnosis and clinical management

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Holoprosencephaly: a guide to diagnosis and clinical management

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Holoprosencephaly: a guide to diagnosis and clinical management

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Indian Pediatrics

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Holoprosencephaly: a guide to diagnosis and clinical management

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Benjamin D Solomon

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Manu S Raam

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Maximilian Muenke

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P2860

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

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

Mutations in the human SIX3 gene in holoprosencephaly are loss of function

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination

Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation.

Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE).

Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients

The molecular genetics of holoprosencephaly.

Holoprosencephaly due to numeric chromosome abnormalities.

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6

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1049269023

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holoprosencephaly

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