Rival JM - Search Results

1

Sonographic findings in Beckwith-Wiedemann syndrome related to H19 hypermethylation.

Le Caignec C, Gicquel C, Gubler MC, Guyot C, You MC, Laurent A, Joubert M, Winer N, David A, Rival JM. Le Caignec C, et al. Among authors: rival jm. Prenat Diagn. 2004 Mar;24(3):165-8. doi: 10.1002/pd.818. Prenat Diagn. 2004. PMID: 15057946

2

Prenatal diagnosis of a small supernumerary, XIST-negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetus.

Le Caignec C, Boceno M, Joubert M, Winer N, Aubron F, Fallet-Bianco C, Rival JM. Le Caignec C, et al. Among authors: rival jm. Prenat Diagn. 2003 Feb;23(2):143-5. doi: 10.1002/pd.553. Prenat Diagn. 2003. PMID: 12575022 Review.

3

Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p.

Le Caignec C, Winer N, Boceno M, Delnatte C, Podevin G, Liet JM, Quere MP, Joubert M, Rival JM. Le Caignec C, et al. Among authors: rival jm. Prenat Diagn. 2003 Dec 15;23(12):981-4. doi: 10.1002/pd.742. Prenat Diagn. 2003. PMID: 14663834 Review.

4

Inherited ring chromosome 8 without loss of subtelomeric sequences.

Le Caignec C, Boceno M, Jacquemont S, Nguyen The Tich S, Rival JM, David A. Le Caignec C, et al. Among authors: rival jm. Ann Genet. 2004 Jul-Sep;47(3):289-96. doi: 10.1016/j.anngen.2003.10.005. Ann Genet. 2004. PMID: 15337475 Review.

5

Two independent rare events--a mutation in the RUNX2 gene and a de novo balanced translocation--in a fetus with cleidocranial dysplasia: pitfall in prenatal diagnosis.

Le Caignec C, Winer N, Philippe HJ, Rival JM. Le Caignec C, et al. Among authors: rival jm. Prenat Diagn. 2006 Aug;26(8):759-60. doi: 10.1002/pd.1499. Prenat Diagn. 2006. PMID: 16865744 No abstract available.

6

Complete sex reversal in a WAGR syndrome patient.

Le Caignec C, Delnatte C, Vermeesch JR, Boceno M, Joubert M, Lavenant F, David A, Rival JM. Le Caignec C, et al. Among authors: rival jm. Am J Med Genet A. 2007 Nov 15;143A(22):2692-5. doi: 10.1002/ajmg.a.31997. Am J Med Genet A. 2007. PMID: 17935232

7

Persisting spongy myocardium. A case indicating the difficulty of antenatal diagnosis.

Winer N, Lefèvre M, Nomballais MF, David A, Rival JM, Gournay V, Debillon T, Rozé JC, Boog G. Winer N, et al. Among authors: rival jm. Fetal Diagn Ther. 1998 Jul-Aug;13(4):227-32. doi: 10.1159/000020843. Fetal Diagn Ther. 1998. PMID: 9784643

8

[The genetics of labio-palatal clefts].

Rival JM, David A. Rival JM, et al. Rev Stomatol Chir Maxillofac. 2001 Jun;102(3-4):171-81. Rev Stomatol Chir Maxillofac. 2001. PMID: 11577471 Review. French.

9

Prenatal diagnosis of a cleidocranial dysplasia-like phenotype associated with a de novo balanced t(2q;6q)(q36;q16) translocation.

Winer N, Le Caignec C, Quere MP, David A, Boceno M, Aubron F, Joubert M, Boog G, Philippe HJ, Rival JM. Winer N, et al. Among authors: rival jm. Ultrasound Obstet Gynecol. 2003 Dec;22(6):648-51. doi: 10.1002/uog.916. Ultrasound Obstet Gynecol. 2003. PMID: 14689542 Free article.

10

46,XY gonadal dysgenesis: evidence for autosomal dominant transmission in a large kindred.

Le Caignec C, Baron S, McElreavey K, Joubert M, Rival JM, Mechinaud F, David A. Le Caignec C, et al. Among authors: rival jm. Am J Med Genet A. 2003 Jan 1;116A(1):37-43. doi: 10.1002/ajmg.a.10820. Am J Med Genet A. 2003. PMID: 12476449

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