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Shprintzen omphalocele syndrome

Known as: PHARYNX AND LARYNX HYPOPLASIA WITH OMPHALOCELE, OMPHALOCELE WITH HYPOPLASIA OF PHARYNX AND LARYNX, LEARNING DISABILITY, DYSMORPHIC FACIES, AND SCOLIOSIS, Shprintzen-Goldberg omphalocele syndrome 
National Institutes of Health

Related topics

Related topics

15 relations
Autosomal dominant inheritanceCongenital EpicanthusCongenital omphaloceleKyphosis deformity of spine

Broader (6)

Congenital exomphalosFaciesLarynxMultiple congenital anomalies

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Innovative Three-Step Microwave-Promoted Synthesis of N-Propargyltetrahydroquinoline and 1,2,3-Triazole Derivatives as a Potential Factor Xa (FXa) Inhibitors: Drug Design, Synthesis, and Biological…
The coagulation cascade is the process of the conversion of soluble fibrinogen to insoluble fibrin that terminates in production… 
2010
2010
OP23.07: Evaluation of umbilical cord insertion site at 9–13 weeks of gestation could predict vasa previa as a screening for placental abnormalities
Results: 33/43 pregnancies (76.7%) were terminated or had spontaneous fetal death due to only chromosomal abnormalities (n = 3; 6… 
Review
2004
Review
2004
Vitamin supplements and the risk for congenital anomalies other than neural tube defects
Randomized trials, supported by many observational studies, have shown that periconceptional use of folic acid, alone or in… 
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