Lacombe D - Search Results

1

Neurodevelopmental outcome following prenatal diagnosis of an isolated anomaly of the corpus callosum.

Mangione R, Fries N, Godard P, Capron C, Mirlesse V, Lacombe D, Duyme M. Mangione R, et al. Among authors: lacombe d. Ultrasound Obstet Gynecol. 2011 Mar;37(3):290-5. doi: 10.1002/uog.8882. Ultrasound Obstet Gynecol. 2011. PMID: 21337654 Free article.

2

Craniofacial dysmorphology and three-dimensional ultrasound: a prospective study on practicability for prenatal diagnosis.

Mangione R, Lacombe D, Carles D, Guyon F, Saura R, Horovitz J. Mangione R, et al. Among authors: lacombe d. Prenat Diagn. 2003 Oct;23(10):810-8. doi: 10.1002/pd.681. Prenat Diagn. 2003. PMID: 14558025

3

Prenatal diagnosis of cerebral and extracerebral high-flow lesions revealing familial capillary malformation-arteriovenous malformation (CM-AVM) syndrome.

Lacalm A, Fichez A, Broussin B, Abel C, Lacombe D, Guibaud L. Lacalm A, et al. Among authors: lacombe d. Ultrasound Obstet Gynecol. 2018 Mar;51(3):409-411. doi: 10.1002/uog.17460. Ultrasound Obstet Gynecol. 2018. PMID: 28295764 Free article. No abstract available.

4

Prenatal diagnosis of hypochondroplasia: three-dimensional multislice computed tomography findings and molecular analysis.

Bonnefoy O, Delbosc JM, Maugey-Laulom B, Lacombe D, Gaye D, Diard F. Bonnefoy O, et al. Among authors: lacombe d. Fetal Diagn Ther. 2006;21(1):18-21. doi: 10.1159/000089042. Fetal Diagn Ther. 2006. PMID: 16354969

5

ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.

Mignot C, Moutard ML, Rastetter A, Boutaud L, Heide S, Billette T, Doummar D, Garel C, Afenjar A, Jacquette A, Lacombe D, Verloes A, Bole-Feysot C, Nitschké P, Masson C, Faudet A, Lesne F, Bienvenu T, Alby C, Attié-Bitach T, Depienne C, Nava C, Héron D. Mignot C, et al. Among authors: lacombe d. Brain. 2016 Nov 1;139(11):e64. doi: 10.1093/brain/aww181. Brain. 2016. PMID: 27474218 No abstract available.

6

New case of Toriello-Carey syndrome.

Lacombe D, Creusot G, Battin J. Lacombe D, et al. Am J Med Genet. 1992 Feb 1;42(3):374-6. doi: 10.1002/ajmg.1320420325. Am J Med Genet. 1992. PMID: 1536182

7

Prenatal diagnosis using array-CGH: a French experience.

Rooryck C, Toutain J, Cailley D, Bouron J, Horovitz J, Lacombe D, Arveiler B, Saura R. Rooryck C, et al. Among authors: lacombe d. Eur J Med Genet. 2013 Jul;56(7):341-5. doi: 10.1016/j.ejmg.2013.02.003. Epub 2013 Feb 20. Eur J Med Genet. 2013. PMID: 23454632 Clinical Trial.

8

X-linked dominant chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia.

Chassaing N, Siani V, Carles D, Delezoide AL, Alberti EM, Battin J, Chateil JF, Gilbert-Dussardier B, Coupry I, Arveiler B, Saura R, Lacombe D. Chassaing N, et al. Among authors: lacombe d. Am J Med Genet A. 2005 Aug 1;136A(4):307-12. doi: 10.1002/ajmg.a.30570. Am J Med Genet A. 2005. PMID: 16001442

9

Reduced placental telomere length during pregnancies complicated by intrauterine growth restriction.

Toutain J, Prochazkova-Carlotti M, Cappellen D, Jarne A, Chevret E, Ferrer J, Idrissi Y, Pelluard F, Carles D, Maugey-Laulon B, Lacombe D, Horovitz J, Merlio JP, Saura R. Toutain J, et al. Among authors: lacombe d. PLoS One. 2013;8(1):e54013. doi: 10.1371/journal.pone.0054013. Epub 2013 Jan 11. PLoS One. 2013. PMID: 23326560 Free PMC article.

10

[Does germinal chromosomal mosaicism exist?].

Goizet C, Taine L, Wen ZQ, Horovitz J, Lacombe D, Saura R. Goizet C, et al. Among authors: lacombe d. J Gynecol Obstet Biol Reprod (Paris). 1997;26(3 Suppl):133-5. J Gynecol Obstet Biol Reprod (Paris). 1997. PMID: 9471442 French. No abstract available.

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