Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies.

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F11%3A7689" target="_blank" >RIV/00064203:_____/11:7689 - isvavai.cz</a>

Alternative codes found

RIV/00216208:11130/11:7689

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies.

Original language description

Hallermann-Streiff syndrome (HSS) is a rare inherited disorder characterized by malformations of the cranium and facial bones, congenital cataracts, microphthalmia, skin atrophy, hypotrichosis, proportionate short stature, teeth abnormalities, and a typical facial appearance with prominent forehead.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

EB - Genetics and molecular biology

OECD FORD branch

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Project

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Continuities

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Publication year

2011

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Molecular Syndromology

ISSN

1661-8769

e-ISSN

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Volume of the periodical

2

Issue of the periodical within the volume

1

Country of publishing house

CH - SWITZERLAND

Number of pages

8

Pages from-to

27-34

UT code for WoS article

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EID of the result in the Scopus database

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