Durand C - 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: durand c. 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: durand c. 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: durand c. 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: durand c. Prenat Diagn. 2004 Feb;24(2):98-100. doi: 10.1002/pd.748. Prenat Diagn. 2004. PMID: 14974114

5

Prenatal presentation of Aicardi-Goutières syndrome: Nonspecific phenotype necessitates exome sequencing for definitive diagnosis.

Bourgon N, Lefebvre M, Kuentz P, Thevenon J, Jouan T, Duffourd Y, Philippe C, Tran Mau-Them F, Durand C, Harizay F, Laurent N, Rousseau T, Faivre L, Thauvin-Robinet C. Bourgon N, et al. Among authors: durand c. Prenat Diagn. 2019 Aug;39(9):806-810. doi: 10.1002/pd.5424. Epub 2019 Feb 20. Prenat Diagn. 2019. PMID: 30681164 No abstract available.

6

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: durand c. Prenat Diagn. 2001 Jun;21(6):466-70. doi: 10.1002/pd.92. Prenat Diagn. 2001. PMID: 11438951

7

Severe fetal cytomegalic inclusion disease after documented maternal reactivation of cytomegalovirus infection during pregnancy.

Rousseau T, Douvier S, Reynaud I, Laurent N, Bour JB, Durand C, Spagnolo G, Sagot P. Rousseau T, et al. Among authors: durand c. Prenat Diagn. 2000 Apr;20(4):333-6. Prenat Diagn. 2000. PMID: 10740207

8

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: durand c. Fetal Diagn Ther. 2002 Jan-Feb;17(1):11-6. doi: 10.1159/000047998. Fetal Diagn Ther. 2002. PMID: 11803209 Review.

9

Recurrence of SOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal mother.

Faivre L, Williamson KA, Faber V, Laurent N, Grimaldi M, Thauvin-Robinet C, Durand C, Mugneret F, Gouyon JB, Bron A, Huet F, Hayward C, Heyningen Vv, Fitzpatrick DR. Faivre L, et al. Among authors: durand c. Am J Med Genet A. 2006 Mar 15;140(6):636-9. doi: 10.1002/ajmg.a.31114. Am J Med Genet A. 2006. PMID: 16470798 No abstract available.

10

17q21.31 microdeletion in a patient with pituitary stalk interruption syndrome.

El Chehadeh-Djebbar S, Callier P, Masurel-Paulet A, Bensignor C, Méjean N, Payet M, Ragon C, Durand C, Marle N, Mosca-Boidron AL, Huet F, Mugneret F, Faivre L, Thauvin-Robinet C. El Chehadeh-Djebbar S, et al. Among authors: durand c. Eur J Med Genet. 2011 May-Jun;54(3):369-73. doi: 10.1016/j.ejmg.2011.03.001. Epub 2011 Mar 30. Eur J Med Genet. 2011. PMID: 21397059

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