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CHD7
LE WE PMID CA
CHD77141CHD7

AEG1

Anophthalmia Esophageal Genital Syndrome

CHARGE syndrome

CHD7

Chromodomain

Esophagus (Atresia)

Feingold syndrome

N Myc

SOX2

Tracheo esophageal fistula (congenital)

VACTERL association

2010  
1
Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome.
[20186815] Am J Med Genet A 152A(3): 674-86 (2010)
2010  
2
Delayed puberty due to a novel mutation in CHD7 causing CHARGE syndrome.
[21041284] Pediatrics 126(6): e1594-8 (2010)
2006  
3
Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology.
[16299066] J Med Genet 43(7): 545-54 (2006)
2010  
4
Chromodomain proteins in development: lessons from CHARGE syndrome.
[20507341] Clin Genet 78(1): 11-20 (2010)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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