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Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of he Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes
Jonathan Eggenschwiler
, Thomas Ludwig
, Peter Fisher
, Philip A. Leighton
, Shirley M. Tilghman
, Argiris Efstratiadis
Molecular Biology
Lewis-Sigler Institute for Integrative Genomics
Princeton School of Public and International Affairs
Research output
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Contribution to journal
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Article
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peer-review
301
Scopus citations
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Dive into the research topics of 'Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of he Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes'. Together they form a unique fingerprint.
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Medicine and Dentistry
Beckwith Wiedemann Syndrome
100%
Simpson Golabi Behmel Syndrome
100%
Chromosome 7
33%
Chromosome Aberration
33%
Somatomedin B Receptor
33%
Omphalocele
33%
Growth Promotor
33%
Chromosome 17
33%
Cleft Palate
33%
Mouse Embryo
33%
Visceromegaly
33%
Keyphrases
Simpson-Golabi-Behmel Syndrome
100%
IGF2R
37%
Visceromegaly
12%
Overgrowth Disorder
12%
Omphalocele
12%
Placentomegaly
12%
11p15.5
12%
Cleft Palate
12%
Biochemistry, Genetics and Molecular Biology
Mouse Mutant
100%
Insulin-Like Growth Factor 2 Receptor
33%