Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1

The role of angiogenic growth factors in organogenesis

(2011) Enrico Crivellato   INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY

Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia

(2011) M. J. Wat et al.   JOURNAL OF MEDICAL GENETICS

Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond-Blackfan anaemia

(2010) M. J. Wat et al.   JOURNAL OF MEDICAL GENETICS

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

(2009) Margaret J. Wat et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Sox7-sustained expression alters the balance between proliferation and differentiation of hematopoietic progenitors at the onset of blood specification

(2009) A. Gandillet et al.   BLOOD

Sox7 and Sox17 are strain-specific modifiers of the lymphangiogenic defects caused by Sox18 dysfunction in mice

(2009) B. Hosking et al.   DEVELOPMENT

Congenital diaphragmatic hernia is part of the new 15q24 microdeletion syndrome

(2009) Hilde Van Esch et al.   European Journal of Medical Genetics

Denys–Drash syndrome and congenital diaphragmatic hernia: Another case with the 1097G > A(Arg366His) mutation

(2008) Timothy Antonius et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Gene expression in the developing diaphragm: significance for congenital diaphragmatic hernia

(2008) Robin D. Clugston et al.   AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY

Establishment of Endoderm Progenitors by SOX Transcription Factor Expression in Human Embryonic Stem Cells

(2008) Cheryle A. Séguin et al.   Cell Stem Cell