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You searched for: Author/Creator Attie‐Bitach, T.

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1. Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia. Issue 6 (29th April 2016)

2. EP08.23: Abnormalities of the fetal corpus callosum: is it time to develop a standard approach?. (30th September 2019)

3. EP23.06: Prenatal diagnosis of Fontaine progeroid syndrome with a de novo mutation in SLC25A24. (14th September 2022)

5. Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatment. (1st April 2022)