Oury JF - Search Results

1

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.

Mornet E, Boue J, Raux-Demay M, Couillin P, Oury JF, Dumez Y, Dausset J, Cohen D, Boué A. Mornet E, et al. Among authors: oury jf. Hum Genet. 1986 Aug;73(4):358-64. doi: 10.1007/BF00279101. Hum Genet. 1986. PMID: 3017844

2

Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes.

Raux-Demay M, Mornet E, Boue J, Couillin P, Oury JF, Ravise N, Deluchat C, Boue A. Raux-Demay M, et al. Among authors: oury jf. Prenat Diagn. 1989 Jul;9(7):457-66. doi: 10.1002/pd.1970090702. Prenat Diagn. 1989. PMID: 2788885

3

Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis.

Boué A, Muller F, Nezelof C, Oury JF, Duchatel F, Dumez Y, Aubry MC, Boué J. Boué A, et al. Among authors: oury jf. Hum Genet. 1986 Nov;74(3):288-97. doi: 10.1007/BF00282551. Hum Genet. 1986. PMID: 3536726

4

Method for first trimester selective abortion in multiple pregnancy.

Dumez Y, Oury JF. Dumez Y, et al. Among authors: oury jf. Contrib Gynecol Obstet. 1986;15:50-3. Contrib Gynecol Obstet. 1986. PMID: 3743080

5

[Prenatal diagnosis of genetic diseases using chorionic villi].

Boué J, Deluchat C, Nicolas H, Oury JF, Dumez Y. Boué J, et al. Among authors: oury jf. J Genet Hum. 1986 Aug;34(3-4):221-33. J Genet Hum. 1986. PMID: 3760827 French.

6

Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21.

Muller F, Rebiffé M, Taillandier A, Oury JF, Mornet E. Muller F, et al. Among authors: oury jf. Hum Genet. 2000 Mar;106(3):340-4. doi: 10.1007/s004390051047. Hum Genet. 2000. PMID: 10798364

7

Prenatal diagnosis of mucolipidosis type II on first-trimester amniotic fluid.

Poenaru L, Mezard C, Akli S, Oury JF, Dumez Y, Boue J. Poenaru L, et al. Among authors: oury jf. Prenat Diagn. 1990 Apr;10(4):231-5. doi: 10.1002/pd.1970100404. Prenat Diagn. 1990. PMID: 1973293

8

First-trimester amniotic fluid acetylcholinesterase electrophoresis.

Muller F, Oury JF, Boue A. Muller F, et al. Among authors: oury jf. Prenat Diagn. 1989 Mar;9(3):173-5. doi: 10.1002/pd.1970090305. Prenat Diagn. 1989. PMID: 2710744

9

First-trimester diagnosis of hypophosphatasia. Importance of gestational age and purity of CV samples.

Muller F, Oury JF, Bussière P, Lewin F, Boué J. Muller F, et al. Among authors: oury jf. Prenat Diagn. 1991 Sep;11(9):725-30. doi: 10.1002/pd.1970110910. Prenat Diagn. 1991. PMID: 1788179

10

Correlation of alkaline phosphatase (ALP) determination and analysis of the tissue non-specific ALP gene in prenatal diagnosis of severe hypophosphatasia.

Mornet E, Muller F, Ngo S, Taillandier A, Simon-Bouy B, Maire I, Oury JF. Mornet E, et al. Among authors: oury jf. Prenat Diagn. 1999 Aug;19(8):755-7. doi: 10.1002/(sici)1097-0223(199908)19:8<755::aid-pd629>3.0.co;2-#. Prenat Diagn. 1999. PMID: 10451522

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

229 results

Search Page

Filters