Concepedia

Searching for genomic variants in IGF2 and CDKN1C in Silver–Russell syndrome patients

Caitriona Obermann, Esther Meyer, Sebastian Prager, Jürgen Tomiuk, H Wollmann, Thomas Eggermann

Molecular Genetics and Metabolism · 2004 · 25 citations · 11 references

DOI

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11

GENEPOP (Version 1.2): Population Genetics Software for Exact Tests and Ecumenicism

Michel Raymond, François Rousset · Journal of Heredity · 1995 · 15.6K citations

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Placental-specific IGF-II is a major modulator of placental and fetal growth

Miguel Constância, Myriam Hemberger, Jennifer Hughes et al. · Nature · 2002 · 1.1K citations

, , +15

Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients

H. A. Wollmann, Teresa Kirchner, H. Enders et al. · European Journal of Pediatrics · 1995 · 205 citations

, , +4

Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion

N. Blagitko · Human Molecular Genetics · 2000 · 179 citations

, , +15

Analysis of germline CDKN1C (p57<sup>KIP2</sup>) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Wayne Lam, Izuho Hatada, Sachiko Oh‐ishi et al. · Journal of Medical Genetics · 1999 · 178 citations · Full text

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