Sagot P - Search Results

1

Prenatal diagnosis of Juberg-Hayward syndrome.

Couvreur-Lionnais S, Rousseau T, Laurent N, Thauvin-Robinet C, Senet-Lacombe E, Delezoïde AL, Mugneret F, Durand C, Faivre L, Sagot P. Couvreur-Lionnais S, et al. Among authors: sagot p. Prenat Diagn. 2005 Feb;25(2):172-5. doi: 10.1002/pd.943. Prenat Diagn. 2005. PMID: 15712337

2

Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome.

Rousseau T, Laurent N, Thauvin-Robinet C, Lionnais S, Durand C, Faivre L, Sagot P. Rousseau T, et al. Among authors: sagot p. Prenat Diagn. 2002 Aug;22(8):692-6. doi: 10.1002/pd.381. Prenat Diagn. 2002. PMID: 12210578

3

Hypomandibular faciocranial dysostosis in consanguineous parents revealed by ultrasound prenatal diagnosis.

Thauvin-Robinet C, Rousseau T, Laurent N, Durand C, Maingueneau C, Cormier-Daire V, Sagot P, Faivre L, Nivelon-Chevallier A. Thauvin-Robinet C, et al. Among authors: sagot p. Prenat Diagn. 2002 Aug;22(8):710-4. doi: 10.1002/pd.385. Prenat Diagn. 2002. PMID: 12210581

4

Prenatal diagnosis of enteric duplication cyst of the tongue.

Rousseau T, Couvreur S, Senet-Lacombe E, Durand C, Justrabo E, Malka G, Sagot P. Rousseau T, et al. Among authors: sagot p. Prenat Diagn. 2004 Feb;24(2):98-100. doi: 10.1002/pd.748. Prenat Diagn. 2004. PMID: 14974114

5

Prenatal overgrowth and mosaic trisomy 15q25-qter including the IGF1 receptor gene.

Faivre L, Rousseau T, Laurent N, Gosset P, Sanlaville D, Thauvin-Robinet C, Cusin V, Lionnais S, Callier P, Khau Van Kien P, Huet F, Turleau C, Sagot P, Mugneret F. Faivre L, et al. Among authors: sagot p. Prenat Diagn. 2004 May;24(5):393-5. doi: 10.1002/pd.891. Prenat Diagn. 2004. PMID: 15164417

6

A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders.

Colombani M, Laurent N, Le Merrer M, Delezoide AL, Thauvin-Robinet C, Huet F, Sagot P, Couvreur S, Rousseau T, Robertson SP, Faivre L. Colombani M, et al. Among authors: sagot p. Prenat Diagn. 2006 Dec;26(12):1151-5. doi: 10.1002/pd.1576. Prenat Diagn. 2006. PMID: 17009344

7

Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephaly.

Thauvin-Robinet C, Rousseau T, Durand C, Laurent N, Maingueneau C, Faivre L, Sagot P, Nivelon-Chevallier A. Thauvin-Robinet C, et al. Among authors: sagot p. Prenat Diagn. 2001 Jun;21(6):466-70. doi: 10.1002/pd.92. Prenat Diagn. 2001. PMID: 11438951

8

Syndromic encephalocele in a fetal case with a 1p35-pter deletion and a 14q32-qter duplication inherited from a maternal balanced translocation.

Thauvin-Robinet C, Callier P, Laurent N, Rousseau T, Masurel-Paulet A, Marle N, Huet F, Sagot P, Faivre L, Mugneret F. Thauvin-Robinet C, et al. Among authors: sagot p. Prenat Diagn. 2007 Jun;27(6):555-9. doi: 10.1002/pd.1724. Prenat Diagn. 2007. PMID: 17385797

9

Contribution of three-dimensional computed tomography in prenatal diagnosis of lethal infantile cortical hyperostosis (Caffey disease).

Darmency V, Thauvin-Robinet C, Rousseau T, Mejean N, Charra S, Coron F, Cassini C, Huet F, Le Merrer M, Cormier-Daire V, Laurent N, Sagot P, Faivre L. Darmency V, et al. Among authors: sagot p. Prenat Diagn. 2009 Sep;29(9):892-4. doi: 10.1002/pd.2302. Prenat Diagn. 2009. PMID: 19455587 No abstract available.

10

Diagnostic and therapeutic dilemma with large prenatally detected cystic adrenal masses.

de Luca JL, Rousseau T, Durand C, Sagot P, Sapin E. de Luca JL, et al. Among authors: sagot p. Fetal Diagn Ther. 2002 Jan-Feb;17(1):11-6. doi: 10.1159/000047998. Fetal Diagn Ther. 2002. PMID: 11803209 Review.

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