Dumez Y - Search Results

1

Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature.

Faivre L, Morichon-Delvallez N, Viot G, Martinovic J, Pinson MP, Aubry JP, Raclin V, Edery P, Dumez Y, Munnich A, Vekemans M. Faivre L, et al. Among authors: dumez y. Prenat Diagn. 1999 Jan;19(1):49-53. Prenat Diagn. 1999. PMID: 10073907 Review.

2

Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.

Faivre L, Morichon-Delvallez N, Viot G, Larget-Piet A, Narcy F, Turleau C, Pinson MP, Dumez Y, Munnich A, Vekemans M. Faivre L, et al. Among authors: dumez y. Prenat Diagn. 1999 Mar;19(3):282-6. Prenat Diagn. 1999. PMID: 10210132 Review.

3

Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency.

Faivre L, Cormier-Daire V, Chrétien D, Christoph von Kleist-Retzow J, Amiel J, Dommergues M, Saudubray JM, Dumez Y, Rötig A, Rustin P, Munnich A. Faivre L, et al. Among authors: dumez y. Prenat Diagn. 2000 Sep;20(9):732-7. doi: 10.1002/1097-0223(200009)20:9<732::aid-pd916>3.0.co;2-#. Prenat Diagn. 2000. PMID: 11015702

4

First-trimester diagnosis of osteogenesis imperfecta associated with encephalocele by conventional and three-dimensional ultrasound.

Ruano R, Picone O, Benachi A, Grebille AG, Martinovic J, Dumez Y, Dommergues M. Ruano R, et al. Among authors: dumez y. Prenat Diagn. 2003 Jul;23(7):539-42. doi: 10.1002/pd.638. Prenat Diagn. 2003. PMID: 12868078

5

A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti.

Steffann J, Raclin V, Smahi A, Woffendin H, Munnich A, Kenwrick SJ, Grebille AG, Benachi A, Dumez Y, Bonnefont JP, Hadj-Rabia S. Steffann J, et al. Among authors: dumez y. Prenat Diagn. 2004 May;24(5):384-8. doi: 10.1002/pd.889. Prenat Diagn. 2004. PMID: 15164415

6

The association of gastroschisis with other congenital anomalies: how important is it?

Ruano R, Picone O, Bernardes L, Martinovic J, Dumez Y, Benachi A. Ruano R, et al. Among authors: dumez y. Prenat Diagn. 2011 Apr;31(4):347-50. doi: 10.1002/pd.2689. Epub 2011 Jan 13. Prenat Diagn. 2011. PMID: 21413033

7

Trisomy 15 in chorionic villi and Prader-Willi syndrome at birth.

Morichon-Delvallez N, Mussat P, Dumez Y, Vekemans M. Morichon-Delvallez N, et al. Among authors: dumez y. Prenat Diagn. 1993 Apr;13(4):307-8. doi: 10.1002/pd.1970130410. Prenat Diagn. 1993. PMID: 8506232 No abstract available.

8

Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up.

Sanlaville D, Aubry MC, Dumez Y, Nolen MC, Amiel J, Pinson MP, Lyonnet S, Munnich A, Vekemans M, Morichon-Delvallez N. Sanlaville D, et al. Among authors: dumez y. J Med Genet. 2000 Jul;37(7):525-8. doi: 10.1136/jmg.37.7.525. J Med Genet. 2000. PMID: 10882756 Free PMC article.

9

Prenatal diagnosis of respiratory chain deficiency by direct mutation screening.

Amiel J, Gigarel N, Benacki A, Benit P, Valnot I, Parfait B, Von Kleist-Retzow JC, Raclin V, Hadj-Rabia S, Dumez Y, Rustin P, Bonnefont JP, Munnich A, Rötig A. Amiel J, et al. Among authors: dumez y. Prenat Diagn. 2001 Jul;21(7):602-4. doi: 10.1002/pd.126. Prenat Diagn. 2001. PMID: 11494300

10

The effect of a systemic arteriovenous fistula on the pulmonary arterial blood pressure in the fetal sheep.

Jouannic JM, Martinovic J, Roussin R, Laborde F, Dumez Y, Dinh-Xuan AT. Jouannic JM, et al. Among authors: dumez y. Prenat Diagn. 2002 Jan;22(1):48-51. doi: 10.1002/pd.255. Prenat Diagn. 2002. PMID: 11810650

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