Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

T. Kosho; N. Okamoto; A.M. van Eerde; [No Value] et al; R.C. Hennekam

Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

Translated title of the contribution: Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

T. Kosho, N. Okamoto, A.M. van Eerde, [No Value] et al, R.C. Hennekam

Department of Genetics

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A
Original language	Undefined/Unknown
Pages (from-to)	262-275
Number of pages	14
Journal	American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
Volume	166c
Issue number	3
Publication status	Published - 2014

Cite this

@article{cd2bbc7526ce4eafbbef0f904e68778d,

title = "Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A",

author = "T. Kosho and N. Okamoto and {van Eerde}, A.M. and {et al}, {[No Value]} and R.C. Hennekam",

year = "2014",

language = "Undefined/Unknown",

volume = "166c",

pages = "262--275",

journal = "American Journal of Medical Genetics. Part C, Seminars in Medical Genetics",

issn = "1552-4868",

publisher = "Wiley-Liss Inc.",

number = "3",

}

TY - JOUR

T1 - Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

AU - Kosho, T.

AU - Okamoto, N.

AU - van Eerde, A.M.

AU - et al, [No Value]

AU - Hennekam, R.C.

PY - 2014

Y1 - 2014

M3 - Article

SN - 1552-4868

VL - 166c

SP - 262

EP - 275

JO - American Journal of Medical Genetics. Part C, Seminars in Medical Genetics

JF - American Journal of Medical Genetics. Part C, Seminars in Medical Genetics

IS - 3

ER -