Congenital hypertelorism and osteopenia: A novel autosomal recessive disease

Carine Bonnard; Barry Merriman; Hane Lee; Hulya Kayserili; Nurten Akarsu; Anna Strobl; Mohammad Shboul; Hanan Hamamy; Bruno Reversade

doi:10.1016/j.diff.2010.09.112

Congenital hypertelorism and osteopenia: A novel autosomal recessive disease

Carine Bonnard
, Barry Merriman
, Hane Lee
, Hulya Kayserili
, Nurten Akarsu
, Anna Strobl
, Mohammad Shboul
, Hanan Hamamy
, Bruno Reversade

Agency for Science Technology & Research (A*STAR)
University of California System
Istanbul University
University of Jordan

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Pages (from-to)	S52-S52
Number of pages	1
Journal	Differentiation
Volume	80
DOIs	https://doi.org/10.1016/j.diff.2010.09.112
Publication status	Published - Nov 2010

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10.1016/j.diff.2010.09.112

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title = "Congenital hypertelorism and osteopenia: A novel autosomal recessive disease",

author = "Carine Bonnard and Barry Merriman and Hane Lee and Hulya Kayserili and Nurten Akarsu and Anna Strobl and Mohammad Shboul and Hanan Hamamy and Bruno Reversade",

year = "2010",

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doi = "10.1016/j.diff.2010.09.112",

language = "English",

volume = "80",

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T2 - A novel autosomal recessive disease

AU - Bonnard, Carine

AU - Merriman, Barry

AU - Lee, Hane

AU - Kayserili, Hulya

AU - Akarsu, Nurten

AU - Strobl, Anna

AU - Shboul, Mohammad

AU - Hamamy, Hanan

AU - Reversade, Bruno

PY - 2010/11

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U2 - 10.1016/j.diff.2010.09.112

DO - 10.1016/j.diff.2010.09.112

M3 - Meeting Abstract

SN - 0301-4681

VL - 80

SP - S52-S52

JO - Differentiation

JF - Differentiation

ER -

Congenital hypertelorism and osteopenia: A novel autosomal recessive disease

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