Till M - Search Results

1

Duplication of chromosome 11 centromere in fetal and maternal karyotypes: a new variant?

Till M, Rafat A, Charrin C, Plauchu H, Germain D. Till M, et al. Prenat Diagn. 1991 Jul;11(7):481-2. doi: 10.1002/pd.1970110713. Prenat Diagn. 1991. PMID: 1754567

2

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.

3

Trisomy 17 mosaicism in amniotic fluid cells not found at birth in blood but present in skin fibroblasts.

Lesca G, Boggio D, Bellec V, Magaud JP, Till M. Lesca G, et al. Among authors: till m. Prenat Diagn. 1999 Mar;19(3):263-5. doi: 10.1002/(sici)1097-0223(199903)19:3<263::aid-pd506>3.0.co;2-0. Prenat Diagn. 1999. PMID: 10210127

4

First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13).

Martin-Denavit T, Attia-Sobol J, Theuil J, Abel-Lablanche K, Boggio D, Teyssier M, Till M, Champion F, Vitrey D, Plauchu H. Martin-Denavit T, et al. Among authors: till m. Prenat Diagn. 2002 Jun;22(6):487-9. doi: 10.1002/pd.343. Prenat Diagn. 2002. PMID: 12116308 No abstract available.

5

Toriello-Carey syndrome and unbalanced translocation t(8;18)(p12;q22).

Martin-Denavit T, Till M, Plauchu H. Martin-Denavit T, et al. Among authors: till m. Am J Med Genet A. 2004 Jul 15;128A(2):219-21. doi: 10.1002/ajmg.a.30043. Am J Med Genet A. 2004. PMID: 15214022 No abstract available.

6

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

7

Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: clinical data and molecular characterization.

Schluth-Bolard C, Till M, Rafat A, Labalme A, Le Lorc'h M, Banquart E, Angei C, Cordier MP, Romana SP, Edery P, Sanlaville D. Schluth-Bolard C, et al. Among authors: till m. Eur J Med Genet. 2008 Nov-Dec;51(6):622-30. doi: 10.1016/j.ejmg.2008.06.009. Epub 2008 Jul 12. Eur J Med Genet. 2008. PMID: 18674648

8

Unexpected diagnosis of 45,X/47,XX,+18 mosaicism in a girl with mild phenotype.

Schluth-Bolard C, Sanlaville D, Labalme A, Till M, Michel-Calemard L, Rafat A, Zabot MT, Nicolino M, Guibaud L, Edery P. Schluth-Bolard C, et al. Among authors: till m. Am J Med Genet A. 2009 Nov;149A(11):2584-7. doi: 10.1002/ajmg.a.32772. Am J Med Genet A. 2009. PMID: 19504602 No abstract available.

9

Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study.

Gruchy N, Blondeel E, Le Meur N, Joly-Hélas G, Chambon P, Till M, Herbaux M, Vigouroux-Castera A, Coussement A, Lespinasse J, Amblard F, Jimenez Pocquet M, Lebel-Roy C, Carré-Pigeon F, Flori E, Mugneret F, Jaillard S, Yardin C, Harbuz R, Collonge-Rame MA, Vago P, Valduga M, Leporrier N, Vialard F. Gruchy N, et al. Among authors: till m. Prenat Diagn. 2016 Jun;36(6):523-9. doi: 10.1002/pd.4817. Epub 2016 May 10. Prenat Diagn. 2016. PMID: 27018091

10

Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences.

Marlet L, Alix E, Till M, Raskin-Champion F, Attia J, Boggio D, Sanlaville D, Schluth-Bolard C. Marlet L, et al. Among authors: till m. Cytogenet Genome Res. 2017;153(3):117-124. doi: 10.1159/000485392. Epub 2017 Dec 22. Cytogenet Genome Res. 2017. PMID: 29268249

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