Encha-Razavi F - Search Results

1

De novo subtelomeric deletion additional to an inherited apparently balanced reciprocal translocation.

Delahaye A, Pipiras E, Kanafani S, Touboul C, Vergnaud A, Encha-Razavi F, Sinico M, Benkhalifa M, Kasakyan S, Serero S, Wolf JP, Gérard-Blanluet M, Benzacken B. Delahaye A, et al. Fetal Diagn Ther. 2007;22(4):306-12. doi: 10.1159/000100797. Epub 2007 Mar 15. Fetal Diagn Ther. 2007. PMID: 17361086

2

Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic images.

Sinico M, Levaillant JM, Vergnaud A, Blondeau JR, Encha-Razavi F, Mornet E, Le Merrer M, Gerard-Blanluet M. Sinico M, et al. Prenat Diagn. 2007 Mar;27(3):222-7. doi: 10.1002/pd.1648. Prenat Diagn. 2007. PMID: 17238218

3

Different proximal and distal rearrangements of chromosome 7q associated with holoprosencephaly.

Benzacken B, Siffroi JP, Le Bourhis C, Krabchi K, Joyé N, Maschino F, Viguié F, Soulié J, Gonzales M, Migné G, Bucourt M, Encha-Razavi F, Carbillon L, Taillemite JL. Benzacken B, et al. J Med Genet. 1997 Nov;34(11):899-903. doi: 10.1136/jmg.34.11.899. J Med Genet. 1997. PMID: 9391882 Free PMC article.

4

Giant omphalocele and "prune belly" sequence as components of the Beckwith-Wiedemann syndrome.

Sinico M, Touboul C, Haddad B, Encha-Razavi F, Paniel JB, Gicquel C, Gérard-Blanluet M. Sinico M, et al. Am J Med Genet A. 2004 Aug 30;129A(2):198-200. doi: 10.1002/ajmg.a.30129. Am J Med Genet A. 2004. PMID: 15316976

5

Excess of neuromuscular spindles in a fetus with Costello syndrome: a clinicopathological report.

Sinico M, Bassez G, Touboul C, Cavé H, Vergnaud A, Zirah C, Fleury-Feith J, Gettler S, Vojtek AM, Chevalier N, Amram D, Alsamad IA, Haddad B, Encha-Razavi F. Sinico M, et al. Pediatr Dev Pathol. 2011 May-Jun;14(3):218-23. doi: 10.2350/09-06-0664-CR.1. Epub 2010 Jul 26. Pediatr Dev Pathol. 2011. PMID: 20658932

6

Prenatal diagnosis and characterization of an analphoid marker chromosome 16.

Tabet AC, Gosset P, Elghezal H, Fontaine S, Martinovic J, Encha Razavi F, Romana S, Vekemans M, Morichon-Delvallez N. Tabet AC, et al. Prenat Diagn. 2004 Sep;24(9):733-6. doi: 10.1002/pd.804. Prenat Diagn. 2004. PMID: 15386469

7

Mosaic trisomy 9 and lobar holoprosencephaly.

Gérard-Blanluet M, Danan C, Sinico M, Lelong F, Borghi E, Dassieu G, Janaud JC, Odent S, Encha-Razavi F. Gérard-Blanluet M, et al. Am J Med Genet. 2002 Aug 15;111(3):295-300. doi: 10.1002/ajmg.10481. Am J Med Genet. 2002. PMID: 12210326

8

Bilateral periventricular heterotopias in an X-linked dominant transmission in a family with two affected males.

Gérard-Blanluet M, Sheen V, Machinis K, Neal J, Apse K, Danan C, Sinico M, Brugières P, Mage K, Ratsimbazafy L, Elbez A, Janaud JC, Amselem S, Walsh C, Encha-Razavi F. Gérard-Blanluet M, et al. Am J Med Genet A. 2006 May 15;140(10):1041-6. doi: 10.1002/ajmg.a.31197. Am J Med Genet A. 2006. PMID: 16596669

9

Arthrogryposis multiplex congenita and cerebellopontine ischemic lesions in sibs: recurrence of prenatal disruptive brain lesions with different patterns of expression?

Mahieu-Caputo D, Salomon LJ, Dommergues M, Aubry MC, Sonigo P, Martinovic Y, Le Merrer M, Dumez Y, Encha-Razavi F. Mahieu-Caputo D, et al. Fetal Diagn Ther. 2002 May-Jun;17(3):153-6. doi: 10.1159/000048029. Fetal Diagn Ther. 2002. PMID: 11914567

10

A practical approach to the examination of the malformed fetal brain: impact on genetic counselling.

Encha-Razavi F, Gonzalès M, Laquerrière A, Martinovic J, Sinico M, Allias F, Bonnière M, Esculpavit C, Gerard M, Attié-Bitach T, Vekemans M. Encha-Razavi F, et al. Pathology. 2008 Feb;40(2):180-7. doi: 10.1080/00313020701813719. Pathology. 2008. PMID: 18203040 Review.

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