References
- Chen CP. 2007. Meckel syndrome: genetics, perinatal findings, and differential diagnosis. Taiwanese Journal of Obstetrics & Gynecology 46:9–14.
- Frantzel O. 1868. Angeborener der Rechten Lungemarterie. Virchows Archiv Pathol Anat 42:420.
- Gottschalk I, Berg C, Heller R. 2012. [Disorders of laterality and heterotaxy in the foetus]. Zeitschrift fur Geburtshilfe und Neonatologie 216:122–131.
- Logan CV, Abdel-Hamed Z, Johnson CA. 2011. Molecular genetics and pathogenic mechanisms for the severe ciliopathies: insights into neurodevelopment and pathogenesis of neural tube defects. Molecular Neurobiology 43:12–26.
- Lurie IW, Prytkov AN, Meldere LV. 1984. Meckel syndrome in different populations. American Journal of Medical Genetics 18:661–669.
- Shetty BP, Alva N, Patil S, Shetty R. 2012. Meckel-Gruber syndrome (dysencephalia splanchnocystica). The Journal of Contemporary Dental Practice 13:713–715.
- Souka AP, Nicolaides KH. 1997. Diagnosis of fetal abnormalities at the 10-14-week scan. Ultrasound in Obstetrics & Gynecology 10:429–442.
- Tanriverdi HA, Hendrik HJ, Ertan K, Schmidt W. 2002. Meckel Gruber syndrome: a first trimester diagnosis of a recurrent case. European Journal of Ultrasound 15:69–72.
- Wright C, Healicon R, English C, Burn J. 1994. Meckel syndrome: what are the minimum diagnostic criteria? Journal of Medical Genetics 31:482–485.