Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the F9

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

4 Citations (Scopus)

14 Downloads (Pure)

Original language	Undefined/Unknown
Pages (from-to)	1220-1224
Number of pages	5
Journal	Molecular genetics & genomic medicine
Volume	6
Issue number	6
DOIs	https://doi.org/10.1002/mgg3.425
Publication status	Published - 2018

Research programs

@article{6274fa1dee2343f8bf7bf877ef3b40ca,

title = "Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the F9",

author = "Carina Stoof and Rogier Kersseboom and Femke Vries and Marieke Kruip and Anneke Kievit and Frank Leebeek",

year = "2018",

doi = "10.1002/mgg3.425",

language = "Undefined/Unknown",

volume = "6",

pages = "1220--1224",

journal = "Molecular genetics & genomic medicine",

issn = "2324-9269",

publisher = "John Wiley & Sons Inc.",

number = "6",

}

TY - JOUR

T1 - Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the F9

AU - Stoof, Carina

AU - Kersseboom, Rogier

AU - Vries, Femke

AU - Kruip, Marieke

AU - Kievit, Anneke

AU - Leebeek, Frank

PY - 2018

Y1 - 2018

U2 - 10.1002/mgg3.425

DO - 10.1002/mgg3.425

M3 - Article

SN - 2324-9269

VL - 6

SP - 1220

EP - 1224

JO - Molecular genetics & genomic medicine

JF - Molecular genetics & genomic medicine

IS - 6

ER -