Premium
Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity
Author(s) -
Giampietro Philip F.,
Babu Deepti,
Zabel Carrie A.,
Silberman Teresa,
Zador Ivan,
DeBauche David,
Ravnan J. Britt,
Dave Bhavana J.
Publication year - 2006
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.31067
Subject(s) - medical genetics , library science , medicine , family medicine , genetics , biology , computer science , gene
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