Premium
Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion
Author(s) -
Natiq Abdelhafid,
Lysy Philippe A.,
Gillemans Nynke,
Schaap Rianne,
Sefiani Abdelaziz,
Amzazi Saaid,
Chafai ElAlaoui Siham,
Cantú Ileana,
Banjanin Bella,
van Lom Kirsten,
Harteveld Cornelis L.,
Philipsen Sjaak
Publication year - 2017
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.24574
Subject(s) - haploinsufficiency , persistence (discontinuity) , fetal hemoglobin , medicine , fetus , genetics , pediatrics , biology , phenotype , gene , pregnancy , geotechnical engineering , engineering
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom