Concepedia

Meckel–Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe

Ingeborg Barišić, Ljubica Boban, Maria Loane, Ester Garne, Diana Wellesley, Elisa Calzolari, Helen Dolk, Marie‐Claude Addor, Jorieke E. H. Bergman, Paula Braz,

European Journal of Human Genetics · 2014 · 85 citations · 29 references

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29

The Meckel syndrome: Clinicopathological findings in 67 patients

Riitta Salonen, John M. Opitz, James F. Reynolds · American Journal of Medical Genetics · 1984 · 204 citations

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Assisted reproductive technology in Europe, 2007: results generated from European registers by ESHRE

J. de Mouzon, V. Goossens, Siladitya Bhattacharya et al. · Human Reproduction · 2012 · 149 citations · Full text

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Spectrum of anomalies in the Meckel syndrome, or: “Maybe there is a malformation syndrome with at least one constant anomaly”

F. Clarke Fraser, Alice Lytwyn, John M. Opitz · American Journal of Medical Genetics · 1981 · 148 citations

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GENETICS OF THE MECKEL SYNDROME (DYSENCEPHALIA SPLANCHNOCYSTICA)

Y. Edward Hsia, Marcel Bratu, A. Herbordt · PEDIATRICS · 1971 · 133 citations

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Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects

Zakia A. Abdelhamed, Gabrielle Wheway, Katarzyna Szymańska et al. · Human Molecular Genetics · 2013 · 108 citations · Full text

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