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Prenatal Diagnosis of Primrose Syndrome.
Abdallah W, Spaggiari E, Brisset S, Dard R, Attié Bitach T, Bault JP, Quibel T. Abdallah W, et al. Among authors: bault jp. J Ultrasound Med. 2024 Feb;43(2):411-414. doi: 10.1002/jum.16354. Epub 2023 Nov 6. J Ultrasound Med. 2024. PMID: 37929614
Cornelia de Lange syndrome: specific features for prenatal diagnosis.
Thellier E, Levaillant JM, Roume J, Quarello E, Bault JP. Thellier E, et al. Among authors: bault jp. Ultrasound Obstet Gynecol. 2017 May;49(5):668-670. doi: 10.1002/uog.15788. Ultrasound Obstet Gynecol. 2017. PMID: 26480950 Free article. No abstract available.
Williams-Beuren syndrome: the prenatal phenotype.
Popowski T, Vialard F, Leroy B, Bault JP, Molina-Gomes D. Popowski T, et al. Among authors: bault jp. Am J Obstet Gynecol. 2011 Dec;205(6):e6-8. doi: 10.1016/j.ajog.2011.09.017. Epub 2011 Sep 24. Am J Obstet Gynecol. 2011. PMID: 22000898
Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder.
Tessarech M, Gorce M, Boussion F, Bault JP, Triau S, Charif M, Khiaty S, Delorme B, Guichet A, Ziegler A, Bris C, Laquerrière A, Fallet-Bianco C, Jacquette A, Salhi H, Héron D, Reynier P, Procaccio V, Bonneau D, Colin E. Tessarech M, et al. Among authors: bault jp. Am J Med Genet A. 2020 Mar;182(3):565-569. doi: 10.1002/ajmg.a.61384. Epub 2019 Dec 3. Am J Med Genet A. 2020. PMID: 31793730
31 results