Boggio D - Search Results

1

[Cystic fibrosis. Fertility and reproduction].

Durieu I, Lepercq J, Rigot JM, Boggio D. Durieu I, et al. Among authors: boggio d. Rev Mal Respir. 2000 Aug;17(3 Pt 2):802-6. Rev Mal Respir. 2000. PMID: 11076390 French.

2

[Male infertility caused by bilateral agenesis of the vas deferens: a new clinical form of cystic fibrosis?].

Durieu I, Bey-Omar F, Rollet J, Boggio D, Bellon G, Morel Y, Vital Durand D. Durieu I, et al. Among authors: boggio d. Rev Med Interne. 1997;18(2):114-8. doi: 10.1016/s0248-8663(97)84676-0. Rev Med Interne. 1997. PMID: 9092029 French.

3

Cystic fibrosis phenotype evaluation and paternity outcome in 50 males with congenital bilateral absence of vas deferens.

Josserand RN, Bey-Omar F, Rollet J, Lejeune H, Boggio D, Durand DV, Durieu I. Josserand RN, et al. Among authors: boggio d. Hum Reprod. 2001 Oct;16(10):2093-7. doi: 10.1093/humrep/16.10.2093. Hum Reprod. 2001. PMID: 11574497

4

Diagnostic criteria for cystic fibrosis in men with congenital absence of the vas deferens.

Durieu I, Bey-Omar F, Rollet J, Calemard L, Boggio D, Lejeune H, Gilly R, Morel Y, Durand DV. Durieu I, et al. Among authors: boggio d. Medicine (Baltimore). 1995 Jan;74(1):42-7. doi: 10.1097/00005792-199501000-00004. Medicine (Baltimore). 1995. PMID: 7837969 Free article.

5

Campomelic acampomelic dysplasia presenting with increased nuchal translucency in the first trimester.

Michel-Calemard L, Lesca G, Morel Y, Boggio D, Plauchu H, Attia-Sobol J. Michel-Calemard L, et al. Among authors: boggio d. Prenat Diagn. 2004 Jul;24(7):519-23. doi: 10.1002/pd.935. Prenat Diagn. 2004. PMID: 15300742

6

Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital.

Pons L, Till M, Alix E, Abel C, Boggio D, Bordes A, Caloone J, Raskin FC, Chatron N, Cordier MP, Fichez A, Labalme A, Lajeunesse C, Liaras É, Massoud M, Miribel J, Ollagnon E, Schluth-Bolard C, Vichier-Cerf A, Edery P, Attia J, Huissoud C, Rudigoz RC, Massardier J, Gaucherand P, Sanlaville D. Pons L, et al. Among authors: boggio d. J Gynecol Obstet Hum Reprod. 2017 Mar;46(3):275-283. doi: 10.1016/j.jogoh.2016.11.004. Epub 2017 Jan 30. J Gynecol Obstet Hum Reprod. 2017. PMID: 28403926

7

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: boggio d. Prenat Diagn. 2002 Jun;22(6):487-9. doi: 10.1002/pd.343. Prenat Diagn. 2002. PMID: 12116308 No abstract available.

8

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: boggio d. Cytogenet Genome Res. 2017;153(3):117-124. doi: 10.1159/000485392. Epub 2017 Dec 22. Cytogenet Genome Res. 2017. PMID: 29268249

9

Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation.

Lesca G, Moizard MP, Bussy G, Boggio D, Hu H, Haas SA, Ropers HH, Kalscheuer VM, Des Portes V, Labalme A, Sanlaville D, Edery P, Raynaud M, Lespinasse J. Lesca G, et al. Among authors: boggio d. Am J Med Genet A. 2013 Dec;161A(12):3063-71. doi: 10.1002/ajmg.a.36162. Epub 2013 Aug 16. Am J Med Genet A. 2013. PMID: 24039113

10

Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome.

Putoux A, Alqahtani A, Pinson L, Paulussen AD, Michel J, Besson A, Mazoyer S, Borg I, Nampoothiri S, Vasiljevic A, Uwineza A, Boggio D, Champion F, de Die-Smulders CE, Gardeitchik T, van Putten WK, Perez MJ, Musizzano Y, Razavi F, Drunat S, Verloes A, Hennekam R, Guibaud L, Alix E, Sanlaville D, Lesca G, Edery P. Putoux A, et al. Among authors: boggio d. Clin Genet. 2016 Dec;90(6):550-555. doi: 10.1111/cge.12781. Epub 2016 Jun 2. Clin Genet. 2016. PMID: 27040866 Free article.

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