NR2F1 haploinsufficiency is associated with optic atrophy, dysmorphism and global developmental delay

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	377-381
Number of pages	5
Journal	American Journal of Medical Genetics, Part A
Volume	161
Issue number	2
DOIs	https://doi.org/10.1002/ajmg.a.35650
State	Published - Feb 2013

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@article{0bbe20d84e6c41c9b46721fcf61f4b27,

title = "NR2F1 haploinsufficiency is associated with optic atrophy, dysmorphism and global developmental delay",

author = "Hussam Al-Kateb and Shimony, \{Joshua S.\} and Marisa Vineyard and Linda Manwaring and Shashikant Kulkarni and Marwan Shinawi",

year = "2013",

month = feb,

doi = "10.1002/ajmg.a.35650",

language = "English",

volume = "161",

pages = "377--381",

journal = "American Journal of Medical Genetics, Part A",

issn = "1552-4825",

number = "2",

}

TY - JOUR

T1 - NR2F1 haploinsufficiency is associated with optic atrophy, dysmorphism and global developmental delay

AU - Al-Kateb, Hussam

AU - Shimony, Joshua S.

AU - Vineyard, Marisa

AU - Manwaring, Linda

AU - Kulkarni, Shashikant

AU - Shinawi, Marwan

PY - 2013/2

Y1 - 2013/2

UR - https://www.scopus.com/pages/publications/84872978049

U2 - 10.1002/ajmg.a.35650

DO - 10.1002/ajmg.a.35650

M3 - Letter

C2 - 23300014

AN - SCOPUS:84872978049

SN - 1552-4825

VL - 161

SP - 377

EP - 381

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 2

ER -