Mittre H - Search Results

1

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.

Claustres M, Guittard C, Bozon D, Chevalier F, Verlingue C, Ferec C, Girodon E, Cazeneuve C, Bienvenu T, Lalau G, Dumur V, Feldmann D, Bieth E, Blayau M, Clavel C, Creveaux I, Malinge MC, Monnier N, Malzac P, Mittre H, Chomel JC, Bonnefont JP, Iron A, Chery M, Georges MD. Claustres M, et al. Among authors: mittre h. Hum Mutat. 2000;16(2):143-56. doi: 10.1002/1098-1004(200008)16:2<143::AID-HUMU7>3.0.CO;2-J. Hum Mutat. 2000. PMID: 10923036

2

CFTR genotypes in patients with normal or borderline sweat chloride levels.

Feldmann D, Couderc R, Audrezet MP, Ferec C, Bienvenu T, Desgeorges M, Claustres M, Mittre H, Blayau M, Bozon D, Malinge MC, Monnier N, Bonnefont JP, Iron A, Bieth E, Dumur V, Clavel C, Cazeneuve C, Girodon E. Feldmann D, et al. Among authors: mittre h. Hum Mutat. 2003 Oct;22(4):340. doi: 10.1002/humu.9183. Hum Mutat. 2003. PMID: 12955726

3

p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study.

René C, Paulet D, Girodon E, Costa C, Lalau G, Leclerc J, Cabet-Bey F, Bienvenu T, Blayau M, Iron A, Mittre H, Feldmann D, Guittard C, Claustres M, Georges Md. René C, et al. Among authors: mittre h. Eur J Hum Genet. 2011 Jan;19(1):36-42. doi: 10.1038/ejhg.2010.137. Epub 2010 Aug 18. Eur J Hum Genet. 2011. PMID: 20717170 Free PMC article.

4

A novel splice mutation, 4006-1G>A, in intron 21 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Mittre H, Duhamel JF, Abeguile G, Lemaire M, Leymarie P. Mittre H, et al. Hum Mutat. 2000 Jan;15(1):121. doi: 10.1002/(SICI)1098-1004(200001)15:1<121::AID-HUMU34>3.0.CO;2-2. Hum Mutat. 2000. PMID: 10612849 No abstract available.

5

A novel nonsense mutation, S466Xa in exon 10 of the cystic fibrosis transmembrane conductance regulator gene.

Mittre H, Barre M, Leymarie P. Mittre H, et al. Hum Mutat. 1996;8(4):392-3. doi: 10.1002/humu.1380080402. Hum Mutat. 1996. PMID: 8956053 No abstract available.

6

A novel nonsense mutation, S434X, in exon 9 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Mittre H, Bahlous A, Leporrier N, Leymarie P. Mittre H, et al. Hum Mutat. 1999 Aug 19;14(2):182. doi: 10.1002/(SICI)1098-1004(1999)14:2<182::AID-HUMU13>3.0.CO;2-V. Hum Mutat. 1999. PMID: 10425081 No abstract available.

7

Genetic counseling for cystic fibrosis: A basic model with new challenges.

Bieth E, Nectoux J, Girardet A, Gruchy N, Mittre H, Laurans M, Guenet D, Brouard J, Gerard M. Bieth E, et al. Among authors: mittre h. Arch Pediatr. 2020 Feb;27 Suppl 1:eS30-eS34. doi: 10.1016/S0929-693X(20)30048-8. Arch Pediatr. 2020. PMID: 32172934 Review.

8

Rapid sequencing of rabbit aromatase cDNA using RACE PCR.

Delarue B, Mittre H, Féral C, Benhaim A, Leymarie P. Delarue B, et al. Among authors: mittre h. C R Acad Sci III. 1996 Aug;319(8):663-70. C R Acad Sci III. 1996. PMID: 8949389

9

Presence of exon I.4 mRNA from CYP19 gene in human granulosa cells.

Bréard E, Roussel H, Lindet Y, Mittre H, Leymarie P. Bréard E, et al. Among authors: mittre h. Mol Cell Endocrinol. 1999 Aug 20;154(1-2):187-90. doi: 10.1016/s0303-7207(99)00083-0. Mol Cell Endocrinol. 1999. PMID: 10509813

10

Correcting for different amplification rates of internal standard and template when measuring cDNA by competitive PCR.

Delarue B, Breard E, Abeguile G, Lemaire M, Mittre H, Leymarie P. Delarue B, et al. Among authors: mittre h. Biotechniques. 2000 Mar;28(3):396-8. doi: 10.2144/00283bm01. Biotechniques. 2000. PMID: 10723547 Free article. No abstract available.

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