Fredouille C - Search Results

1

Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literature.

Sigaudy S, Toutain A, Moncla A, Fredouille C, Bourlière B, Ayme S, Philip N. Sigaudy S, et al. Among authors: fredouille c. Am J Med Genet. 1998 Oct 30;80(1):16-24. Am J Med Genet. 1998. PMID: 9800907 Review.

2

Neonatal death in Marshall-Smith syndrome.

Chatel C, Maazoul F, Sigaudy S, Fredouille C, Ayme S, Philip N. Chatel C, et al. Among authors: fredouille c. Genet Couns. 1998;9(1):15-8. Genet Couns. 1998. PMID: 9555581

3

Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2.

Sigaudy S, Moncla A, Fredouille C, Bourlière B, Lambert JC, Philip N. Sigaudy S, et al. Among authors: fredouille c. Clin Dysmorphol. 1998 Oct;7(4):257-62. doi: 10.1097/00019605-199810000-00004. Clin Dysmorphol. 1998. PMID: 9823491

4

Prenatal ultrasonographic findings in Proteus syndrome.

Sigaudy S, Fredouille C, Gambarelli D, Potier A, Cassin D, Piquet C, Philip N. Sigaudy S, et al. Among authors: fredouille c. Prenat Diagn. 1998 Oct;18(10):1091-4. Prenat Diagn. 1998. PMID: 9826904

5

Value of fetal skeletal radiographs in the diagnosis of fetal death.

Bourlière-Najean B, Russel AS, Panuel M, Piercecchi-Marti MD, Sigaudy S, Fredouille C, Petit P, Philip N, Devred P. Bourlière-Najean B, et al. Among authors: fredouille c. Eur Radiol. 2003 May;13(5):1046-9. doi: 10.1007/s00330-002-1474-3. Epub 2002 Jul 4. Eur Radiol. 2003. PMID: 12695826

6

Tetra-amelia and lung aplasia syndrome: report of a new family and exclusion of candidate genes.

Krahn M, Julia S, Sigaudy S, Liprandi A, Bernard R, Gonnet K, Heuertz S, Bonaventure J, Chau C, Fredouille C, Levy N, Philip N. Krahn M, et al. Among authors: fredouille c. Clin Genet. 2005 Dec;68(6):558-60. doi: 10.1111/j.1399-0004.2005.00531.x. Clin Genet. 2005. PMID: 16283889 No abstract available.

7

Value of fetal autopsy after medical termination of pregnancy.

Piercecchi-Marti MD, Liprandi A, Sigaudy S, Fredouille C, Adalian P, Figarella-Branger D, Pellissier JF. Piercecchi-Marti MD, et al. Among authors: fredouille c. Forensic Sci Int. 2004 Aug 11;144(1):7-10. doi: 10.1016/j.forsciint.2004.01.022. Forensic Sci Int. 2004. PMID: 15240015

8

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

Sanlaville D, Etchevers HC, Gonzales M, Martinovic J, Clément-Ziza M, Delezoide AL, Aubry MC, Pelet A, Chemouny S, Cruaud C, Audollent S, Esculpavit C, Goudefroye G, Ozilou C, Fredouille C, Joye N, Morichon-Delvallez N, Dumez Y, Weissenbach J, Munnich A, Amiel J, Encha-Razavi F, Lyonnet S, Vekemans M, Attié-Bitach T. Sanlaville D, et al. Among authors: fredouille c. J Med Genet. 2006 Mar;43(3):211-217. doi: 10.1136/jmg.2005.036160. Epub 2005 Sep 16. J Med Genet. 2006. PMID: 16169932 Free PMC article.

9

[Diagnosis of a fetal cardiac malformation. Fetal heart].

Fredouille C. Fredouille C. Ann Pathol. 1997 Sep;17(4):300-5. Ann Pathol. 1997. PMID: 9409892 Review. French.

10

Congenital atrioventricular block: histological aspects.

Piercecchi-Marti MD, Mohamed H, Chau C, Liprandi A, Fredouille C. Piercecchi-Marti MD, et al. Among authors: fredouille c. Forensic Sci Int. 2003 Sep 9;136(1-3):12-5. doi: 10.1016/s0379-0738(03)00224-x. Forensic Sci Int. 2003. PMID: 12969615

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