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Toriello-Carey syndrome.
Till M, Bourgeois J, Plauchu H. Till M, et al. Am J Med Genet. 1997 Jun 13;70(3):332. doi: 10.1002/(sici)1096-8628(19970613)70:3<332::aid-ajmg23>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9188677 No abstract available.
Prenatal diagnosis of Aicardi-Goutières syndrome.
Le Garrec M, Doret M, Pasquier JC, Till M, Lebon P, Buenerd A, Escalon J, Gaucherand P. Le Garrec M, et al. Among authors: till m. Prenat Diagn. 2005 Jan;25(1):28-30. doi: 10.1002/pd.881. Prenat Diagn. 2005. PMID: 15662687
Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Guterman S, Beneteau C, Redon S, Dupont C, Missirian C, Jaeger P, Herve B, Jacquin C, Douet-Guilbert N, Till M, Tabet AC, Moradkhani K, Malan V, Doco-Fenzy M, Vialard F. Guterman S, et al. Among authors: till m. Prenat Diagn. 2019 Sep;39(10):871-882. doi: 10.1002/pd.5498. Epub 2019 Jul 5. Prenat Diagn. 2019. PMID: 31172545 Review.
TWIST microdeletion identified by array CGH in a patient presenting Saethre-Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7.
Schluth-Bolard C, Till M, Labalme A, Rey C, Banquart E, Fautrelle A, Martin-Denavit T, Le Lorc'h M, Romana SP, Lazar V, Edery P, Sanlaville D. Schluth-Bolard C, et al. Among authors: till m. Eur J Med Genet. 2008 Mar-Apr;51(2):156-64. doi: 10.1016/j.ejmg.2007.12.003. Epub 2007 Dec 24. Eur J Med Genet. 2008. PMID: 18255367
258 results