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2. Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomalies. Issue 5 (21st April 2018)

3. Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation. Issue 18 (7th September 2021)

5. Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype?. Issue 6 (14th September 2020)

6. Fetal megacystis‐microcolon: Genetic mutational spectrum and identification of PDCL3 as a novel candidate gene. Issue 3 (4th August 2020)

10. Fetal Cerebral Ventricular Dilatation: Etiopathogenic Study of 130 Observations. Issue 19 (31st July 2017)