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Microdeletion of 7p12.1p13, including IKZF 1 , causes intellectual impairment, overgrowth, and susceptibility to leukaemia
Author(s) -
Järviaho Tekla,
Zachariadis Vasilios,
Tesi Bianca,
Chiang Samuel,
Bryceson Yenan T.,
Möttönen Merja,
Niinimäki Riitta,
Bang Benedicte,
Rahikkala Elisa,
Taylan Fulya,
Uusimaa Johanna,
HarilaSaari Arja,
Nordgren Ann
Publication year - 2019
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.15494
Subject(s) - medicine , hypertelorism , germline mutation , sibling , germline , hematopoietic stem cell transplantation , genetic predisposition , transplantation , immunology , disease , genetics , pathology , biology , mutation , gene , psychology , developmental psychology , anatomy
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