Devisme L - Search Results

1

New autosomal recessive syndrome of severe microcephaly and skeletal anomalies including posterior rib-gap defects.

Duval A, Boute O, Devisme L, Valat AS, Manouvrier S. Duval A, et al. Among authors: devisme l. Am J Med Genet. 1998 Dec 4;80(4):429-34. Am J Med Genet. 1998. PMID: 9856577

2

Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: a new X-linked dominant multiple congenital anomalies syndrome?

Manouvrier S, Moerman A, Coeslier A, Devisme L, Boute O, Le Merrer M. Manouvrier S, et al. Among authors: devisme l. Am J Med Genet. 2000 Feb 28;90(5):351-5. doi: 10.1002/(sici)1096-8628(20000228)90:5<351::aid-ajmg1>3.0.co;2-k. Am J Med Genet. 2000. PMID: 10706353

3

Pre- and postnatal diagnosis of limb anomalies: a series of 107 cases.

Holder-Espinasse M, Devisme L, Thomas D, Boute O, Vaast P, Fron D, Herbaux B, Puech F, Manouvrier-Hanu S. Holder-Espinasse M, et al. Among authors: devisme l. Am J Med Genet A. 2004 Feb 1;124A(4):417-22. doi: 10.1002/ajmg.a.20359. Am J Med Genet A. 2004. PMID: 14735595 Review.

4

Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum: case report and review of the literature.

Andrieux J, Devisme L, Valat AS, Robert Y, Frnka C, Savary JB. Andrieux J, et al. Among authors: devisme l. Eur J Med Genet. 2005 Apr-Jun;48(2):199-206. doi: 10.1016/j.ejmg.2005.01.028. Epub 2005 Feb 12. Eur J Med Genet. 2005. PMID: 16053913 Review.

5

[Cerebral fetal MRI and ventriculomegaly].

Launay S, Robert Y, Valat AS, Thomas D, Devisme L, Rocourt N, Vaast P. Launay S, et al. Among authors: devisme l. J Radiol. 2002 Jun;83(6 Pt 1):723-30. J Radiol. 2002. PMID: 12149589 French.

6

[Sirenomelia as a part of VACTERL association: a study of three cases].

Charlier P, Valat AS, Boute O, Petit S, Chafiotte C, Huynh-Charlier I, Gosselin B, Devisme L. Charlier P, et al. Among authors: devisme l. Ann Pathol. 2008 Jun;28(3):176-81. doi: 10.1016/j.annpat.2008.06.001. Epub 2008 Jul 22. Ann Pathol. 2008. PMID: 18706355 French.

7

Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe Silver-Russell syndrome.

Ghanim M, Rossignol S, Delobel B, Irving M, Miller O, Devisme L, Plennevaux JL, Lucidarme-Rossi S, Manouvrier S, Salah A, Chivu O, Netchine I, Vincent-Delorme C. Ghanim M, et al. Among authors: devisme l. Am J Med Genet A. 2013 Mar;161A(3):572-7. doi: 10.1002/ajmg.a.35691. Epub 2013 Feb 7. Am J Med Genet A. 2013. PMID: 23401077

8

Phenotypic variability of prenatally presenting Gaucher's disease.

Beaujot J, Joriot S, Dieux A, Vaast P, Franquet-Ansart H, Valat AS, Deruelle P, Holder-Espinasse M, Devisme L. Beaujot J, et al. Among authors: devisme l. Prenat Diagn. 2013 Oct;33(10):1004-6. doi: 10.1002/pd.4171. Epub 2013 Jul 4. Prenat Diagn. 2013. PMID: 23749476 No abstract available.

9

The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.

Ghesh L, Musquer MD, Devisme L, Stichelbout M, Boutaud L, Elkhartoufi N, Vaast P, Boute O, Riteau AS, Le Vaillant C, Winer N, Joubert M, Bezieau S, Thomas S, Attie-Bitach T, Beneteau C. Ghesh L, et al. Among authors: devisme l. Clin Genet. 2021 Oct;100(4):462-467. doi: 10.1111/cge.14021. Epub 2021 Jul 13. Clin Genet. 2021. PMID: 34212369

10

[An ischemic pulmonary malformation of the surviving fetus occurring after selective embryo reduction in bichorionic pregnancy. Report of one case and literature review].

Jemmali M, Devisme L, Valat AS, Boute O, Vaast P, Subtil D, Puech F. Jemmali M, et al. Among authors: devisme l. J Gynecol Obstet Biol Reprod (Paris). 2001 Sep;30(5):467-72. J Gynecol Obstet Biol Reprod (Paris). 2001. PMID: 11598561 Free article. Review. French.

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