Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

41 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[Trisomy 18: ultrasound aspects. Report of 40 cases].
Brun L, Dufour P, Savary JB, Valat AS, Boute O, Subtil D, Vaast P, Bourgeot P, Manouvrier S, de Martinville B, Puech F. Brun L, et al. Among authors: de martinville b. Presse Med. 2000 Dec 9;29(38):2082-6. Presse Med. 2000. PMID: 11147045 French.
[Prenatal diagnosis of partial trisomy 9p].
Vanderstichele S, Savary JB, Dufour P, Berard J, Tordjeman N, Vinatier D, Monnier JC, de Martinville B. Vanderstichele S, et al. Among authors: de martinville b. J Gynecol Obstet Biol Reprod (Paris). 1997;26(6):630-2. J Gynecol Obstet Biol Reprod (Paris). 1997. PMID: 9453981 Free article. French.
[Marfan syndrome and pregnancy. Apropos of 4 cases].
Lambaudie E, Depret-Mosser S, Occelli B, Papageorgiou T, Dognin A, Bertrand M, de Martinville B, Codaccioni X, Monnier JC. Lambaudie E, et al. Among authors: de martinville b. Gynecol Obstet Fertil. 2002 Jul-Aug;30(7-8):567-75. doi: 10.1016/s1297-9589(02)00379-x. Gynecol Obstet Fertil. 2002. PMID: 12199039 French.
Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.
Tuffery-Giraud S, Béroud C, Leturcq F, Yaou RB, Hamroun D, Michel-Calemard L, Moizard MP, Bernard R, Cossée M, Boisseau P, Blayau M, Creveaux I, Guiochon-Mantel A, de Martinville B, Philippe C, Monnier N, Bieth E, Khau Van Kien P, Desmet FO, Humbertclaude V, Kaplan JC, Chelly J, Claustres M. Tuffery-Giraud S, et al. Among authors: de martinville b. Hum Mutat. 2009 Jun;30(6):934-45. doi: 10.1002/humu.20976. Hum Mutat. 2009. PMID: 19367636
Attenuated presentation of ataxia-telangiectasia with familial cancer history.
Simonin C, Devos D, Vuillaume I, de Martinville B, Sablonnière B, Destée A, Stoppa-Lyonnet D, Defebvre L. Simonin C, et al. Among authors: de martinville b. J Neurol. 2008 Aug;255(8):1261-3. doi: 10.1007/s00415-008-0857-z. Epub 2008 Jun 30. J Neurol. 2008. PMID: 18575927 No abstract available.
The clinical spectrum associated with a chromosome 17 short arm proximal duplication (dup 17p11.2) in three patients.
Doco-Fenzy M, Holder-Espinasse M, Bieth E, Magdelaine C, Vincent MC, Khoury M, Andrieux J, Zhang F, Lupski JR, Klink R, Schneider A, Goze-Martineau O, Cuisset JM, Vallee L, Manouvrier-Hanu S, Gaillard D, de Martinville B. Doco-Fenzy M, et al. Among authors: de martinville b. Am J Med Genet A. 2008 Apr 1;146A(7):917-24. doi: 10.1002/ajmg.a.32195. Am J Med Genet A. 2008. PMID: 18327785
41 results