Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement ofFOXG1appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus-Reference-Cited by-同舟云学术

Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement ofFOXG1appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus

Published:2012-05-25 Issue:6 Volume:49 Page:366-372
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Santen Gijs W E,Sun Yu,Gijsbers Antoinet C J,Carré Aurore,Holvoet Maureen,Haeringen Arie van,Lesnik Oberstein Saskia A J,Tomoda Akemi,Mabe Hiroyo,Polak Michel,Devriendt Koenraad,Ruivenkamp Claudia A L,Bijlsma Emilia K

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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