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1.
Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.
Hum Mol Genet
; 21(18): 4115-25, 2012 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22723016
2.
Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.
J Med Genet
; 48(5): 299-307, 2011 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-21525063
3.
Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia.
J Med Genet
; 47(11): 777-81, 2010 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-20921022
4.
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
Am J Med Genet A
; 149A(8): 1661-77, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19606479
5.
Sox7 in vascular development: review, insights and potential mechanisms.
Int J Dev Biol
; 58(1): 1-8, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24860989
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