Results 151 to 160 of about 9,070 (214)

Clinical application and systematic review of waiting treatment for giant omphaloceles. [PDF]

open access: yesBMC Pediatr
Pan R   +8 more
europepmc   +1 more source

CRISPR-Cas9-Generated TXNDC15 c.560delA Homozygous Mouse Model Exhibits Meckel-Gruber Syndrome Phenotype. [PDF]

open access: yesGenesis
Liu Y   +10 more
europepmc   +1 more source

Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphalocele. [PDF]

open access: yesFront Cell Dev Biol
Kolvenbach CM   +11 more
europepmc   +1 more source

Omphalocele

open access: yes, 2005
Stig Sømme, Jacob C. Langer
openaire   +1 more source

Hand1 gene replacement with Hand2 reveals overlap in function with unique occurrence of omphalocele and heart defects. [PDF]

open access: yesDevelopment
Firulli BA   +7 more
europepmc   +1 more source

Clinical phenotype and molecular genetic analysis of 24 cases of Beckwith-Wiedemann syndrome. [PDF]

open access: yesTransl Pediatr
Wu Z   +9 more
europepmc   +1 more source

Omphalocele.

open access: yesClinical proceedings - Children's Hospital of the District of Columbia, 2003
openaire   +3 more sources

Challenges in prenatal care of ectopic cordis: Case series and literature review. [PDF]

open access: yesRadiol Case Rep
Martadiansyah A   +8 more
europepmc   +1 more source

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