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

Author:

Barisic Ingeborg,Boban Ljubica,Loane Maria,Garne Ester,Wellesley Diana,Calzolari Elisa,Dolk Helen,Addor Marie-Claude,Bergman Jorieke EH,Braz Paula,Draper Elizabeth S,Haeusler Martin,Khoshnood Babak,Klungsoyr Kari,Pierini Anna,Queisser-Luft Annette,Rankin Judith,Rissmann Anke,Verellen-Dumoulin Christine

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference39 articles.

1. Meckel JF : Beschreibung zweier, durch sehr aehnliche Bildungsabweichungen entstellter Geschwister. Dtsch Arch Physiol 1822; 7: 99–172.

2. Opitz JM, Howe JJ : The Meckel syndrome (dysencephalia splanchnocystica, the Gruber Syndrome). Birth Defects 1969; 2: 167–179.

3. Mecke S, Passarge E : Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome. Ann Genet 1971; 14: 97–103.

4. Hsia YE, Bratu M, Herbordt A : Genetics of the Meckel syndrome (dysencephalia splanchnocystica). Pediatrics 1971; 48: 237–247.

5. Fraser FC, Lytwyn A : Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly". Am J Med Genet 1981; 9: 67–73.

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