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

109 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Prenatal diagnosis of fetal tail and postabortum anatomical description.
Grangé G, Tantau J, Pannier E, Aubry MC, Viot G, Fallet-Bianco C, Terrasse G, Cabrol D. Grangé G, et al. Ultrasound Obstet Gynecol. 2001 Nov;18(5):531-3. doi: 10.1046/j.0960-7692.2001.00529.x. Ultrasound Obstet Gynecol. 2001. PMID: 11844178 Free article.
Fetal intracerebral hemorrhage in familial thrombophilia.
Crespin M, Alhenc-Gelas M, Grangé G, Fallet-Bianco C, Fontenay M. Crespin M, et al. Pediatr Neurol. 2009 Oct;41(4):291-3. doi: 10.1016/j.pediatrneurol.2009.04.027. Pediatr Neurol. 2009. PMID: 19748050
A new case of exomphalos, short limbs, and macrogonadism syndrome.
Viot G, Pannier E, Faivre L, Tantau J, Fallet-Bianco C, Dupont JM, Jouannet P, Aubry MC, Lyonnet S, Cabrol D. Viot G, et al. J Med Genet. 2001 Mar;38(3):E8. doi: 10.1136/jmg.38.3.e8. J Med Genet. 2001. PMID: 11238685 Free PMC article. No abstract available.
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations.
Legendre M, Gonzales M, Goudefroye G, Bilan F, Parisot P, Perez MJ, Bonnière M, Bessières B, Martinovic J, Delezoide AL, Jossic F, Fallet-Bianco C, Bucourt M, Tantau J, Loget P, Loeuillet L, Laurent N, Leroy B, Salhi H, Bigi N, Rouleau C, Guimiot F, Quélin C, Bazin A, Alby C, Ichkou A, Gesny R, Kitzis A, Ville Y, Lyonnet S, Razavi F, Gilbert-Dussardier B, Vekemans M, Attié-Bitach T. Legendre M, et al. J Med Genet. 2012 Nov;49(11):698-707. doi: 10.1136/jmedgenet-2012-100926. Epub 2012 Sep 28. J Med Genet. 2012. PMID: 23024289
Matthew-Wood syndrome: report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2.
Martinovic-Bouriel J, Bernabé-Dupont C, Golzio C, Grattagliano-Bessières B, Malan V, Bonnière M, Esculpavit C, Fallet-Bianco C, Mirlesse V, Le Bidois J, Aubry MC, Vekemans M, Morichon N, Etchevers H, Attié-Bitach T, Encha-Razavi F, Benachi A. Martinovic-Bouriel J, et al. Am J Med Genet A. 2007 Feb 1;143A(3):219-28. doi: 10.1002/ajmg.a.31599. Am J Med Genet A. 2007. PMID: 17236193
109 results