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Items: 1 to 50 of 79

1.

Dynein-mediated transport and membrane trafficking control PAR3 polarised distribution.

Jouette J, Guichet A, Claret SB.

Elife. 2019 Jan 23;8. pii: e40212. doi: 10.7554/eLife.40212.

2.

High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5.

Lerat J, Bonnet C, Cartault F, Loundon N, Jacquemont ML, Darcel F, Rouillon I, Mezouaghi K, Guichet A, Litzler J, Gesny R, Gherbi S, Aissa IB, Digeon FSJ, Garabedian EN, Bonnefont JP, Genin E, Denoyelle F, Jonard L, Marlin S.

Clin Genet. 2019 Jan;95(1):177-181. doi: 10.1111/cge.13460. Epub 2018 Nov 4.

PMID:
30298622
3.

New case of bilateral pheochromocytomas involving the homozygous TMEM127 mutation.

Laboureau S, Guichet A, Duriez T, Veyrat-Durebex C, Bouzamondo N, Briet C, Mirebeau-Prunier D.

Clin Genet. 2018 Aug;94(2):278-279. doi: 10.1111/cge.13361. Epub 2018 May 11. No abstract available.

PMID:
29749617
4.

Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia.

Moortgat S, Lederer D, Deprez M, Buzatu M, Clapuyt P, Boulanger S, Benoit V, Mary S, Guichet A, Ziegler A, Colin E, Bonneau D, Maystadt I.

Eur J Med Genet. 2018 Mar 3. pii: S1769-7212(17)30666-3. doi: 10.1016/j.ejmg.2018.03.002. [Epub ahead of print] Review.

PMID:
29510240
5.

Genetic analysis of adults heterozygous for ALPL mutations.

Taillandier A, Domingues C, Dufour A, Debiais F, Guggenbuhl P, Roux C, Cormier C, Cortet B, Porquet-Bordes V, Coury F, Geneviève D, Chiesa J, Colin T, Fletcher E, Guichet A, Javier RM, Laroche M, Laurent M, Lausch E, LeHeup B, Lukas C, Schwabe G, van der Burgt I, Muti C, Simon-Bouy B, Mornet E.

J Bone Miner Metab. 2018 Nov;36(6):723-733. doi: 10.1007/s00774-017-0888-6. Epub 2017 Dec 13.

PMID:
29236161
6.

Nucleus positioning within Drosophila egg chamber.

Bernard F, Lepesant JA, Guichet A.

Semin Cell Dev Biol. 2018 Oct;82:25-33. doi: 10.1016/j.semcdb.2017.10.013. Epub 2017 Oct 19. Review.

PMID:
29056490
7.

Phosphoinositides and Cell Polarity in the Drosophila Egg Chamber.

Jouette J, Claret S, Guichet A.

Results Probl Cell Differ. 2017;63:169-187. doi: 10.1007/978-3-319-60855-6_8.

PMID:
28779318
8.

Distinct molecular cues ensure a robust microtubule-dependent nuclear positioning in the Drosophila oocyte.

Tissot N, Lepesant JA, Bernard F, Legent K, Bosveld F, Martin C, Faklaris O, Bellaïche Y, Coppey M, Guichet A.

Nat Commun. 2017 Apr 27;8:15168. doi: 10.1038/ncomms15168.

9.

Reliance of Wolbachia on High Rates of Host Proteolysis Revealed by a Genome-Wide RNAi Screen of Drosophila Cells.

White PM, Serbus LR, Debec A, Codina A, Bray W, Guichet A, Lokey RS, Sullivan W.

Genetics. 2017 Apr;205(4):1473-1488. doi: 10.1534/genetics.116.198903. Epub 2017 Feb 3.

10.

Methods to Establish Drosophila Cell Lines.

Debec A, Megraw TL, Guichet A.

Methods Mol Biol. 2016;1478:333-351. Review.

PMID:
27730593
11.

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease.

Davignon L, Chauveau C, Julien C, Dill C, Duband-Goulet I, Cabet E, Buendia B, Lilienbaum A, Rendu J, Minot MC, Guichet A, Allamand V, Vadrot N, Fauré J, Odent S, Lazaro L, Leroy JP, Marcorelles P, Dubourg O, Ferreiro A.

Hum Mol Genet. 2016 Apr 15;25(8):1559-73. doi: 10.1093/hmg/ddw033. Epub 2016 Feb 9.

PMID:
27008887
12.

Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45.

Fradin M, Colin E, Hannouche-Bared D, Audo I, Sahel JA, Biskup S, Carré W, Ziegler A, Wilhelm C, Guichet A, Odent S, Bonneau D.

Ophthalmic Genet. 2016 Sep;37(3):357-9. doi: 10.3109/13816810.2015.1087578. Epub 2016 Feb 22. No abstract available.

13.

In Utero Diagnosis of Niemann-Pick Type C in the Absence of Family History.

Colin E, Barth M, Boussion F, Latour P, Piguet-Lacroix G, Guichet A, Ziegler A, Triau S, Loisel D, Sentilhes L, Bonneau D.

JIMD Rep. 2016;28:105-110. Epub 2015 Nov 14.

14.

Visualizing Microtubule Networks During Drosophila Oogenesis Using Fixed and Live Imaging.

Legent K, Tissot N, Guichet A.

Methods Mol Biol. 2015;1328:99-112. doi: 10.1007/978-1-4939-2851-4_7.

PMID:
26324432
15.

New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Pilliod J, Moutton S, Lavie J, Maurat E, Hubert C, Bellance N, Anheim M, Forlani S, Mochel F, N'Guyen K, Thauvin-Robinet C, Verny C, Milea D, Lesca G, Koenig M, Rodriguez D, Houcinat N, Van-Gils J, Durand CM, Guichet A, Barth M, Bonneau D, Convers P, Maillart E, Guyant-Marechal L, Hannequin D, Fromager G, Afenjar A, Chantot-Bastaraud S, Valence S, Charles P, Berquin P, Rooryck C, Bouron J, Brice A, Lacombe D, Rossignol R, Stevanin G, Benard G, Burglen L, Durr A, Goizet C, Coupry I.

Ann Neurol. 2015 Dec;78(6):871-86. doi: 10.1002/ana.24509. Epub 2015 Nov 14.

PMID:
26288984
16.

Treacher Collins syndrome: a clinical and molecular study based on a large series of patients.

Vincent M, Geneviève D, Ostertag A, Marlin S, Lacombe D, Martin-Coignard D, Coubes C, David A, Lyonnet S, Vilain C, Dieux-Coeslier A, Manouvrier S, Isidor B, Jacquemont ML, Julia S, Layet V, Naudion S, Odent S, Pasquier L, Pelras S, Philip N, Pierquin G, Prieur F, Aboussair N, Attie-Bitach T, Baujat G, Blanchet P, Blanchet C, Dollfus H, Doray B, Schaefer E, Edery P, Giuliano F, Goldenberg A, Goizet C, Guichet A, Herlin C, Lambert L, Leheup B, Martinovic J, Mercier S, Mignot C, Moutard ML, Perez MJ, Pinson L, Puechberty J, Willems M, Randrianaivo H, Szakszon K, Toutain A, Verloes A, Vigneron J, Sanchez E, Sarda P, Laplanche JL, Collet C.

Genet Med. 2016 Jan;18(1):49-56. doi: 10.1038/gim.2015.29. Epub 2015 Mar 19. Erratum in: Genet Med. 2015 Aug;17(8):686. Szaskon, Kateline [corrected to Szakszon, Kateline].

PMID:
25790162
17.

Microtubule-dependent apical restriction of recycling endosomes sustains adherens junctions during morphogenesis of the Drosophila tracheal system.

Le Droguen PM, Claret S, Guichet A, Brodu V.

Development. 2015 Jan 15;142(2):363-74. doi: 10.1242/dev.113472.

18.

Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome.

Colin E, Huynh Cong E, Mollet G, Guichet A, Gribouval O, Arrondel C, Boyer O, Daniel L, Gubler MC, Ekinci Z, Tsimaratos M, Chabrol B, Boddaert N, Verloes A, Chevrollier A, Gueguen N, Desquiret-Dumas V, Ferré M, Procaccio V, Richard L, Funalot B, Moncla A, Bonneau D, Antignac C.

Am J Hum Genet. 2014 Dec 4;95(6):637-48. doi: 10.1016/j.ajhg.2014.10.011. Epub 2014 Nov 13.

19.

Extensive Mongolian spots in 4p16.3 deletion (Wolf-Hirschhorn syndrome).

Ziegler A, Guichet A, Pinson L, Barth M, Levade T, Bonneau D, Colin E.

Clin Dysmorphol. 2014 Jul;23(3):109-10. doi: 10.1097/MCD.0000000000000041. No abstract available.

PMID:
24859493
20.

PI(4,5)P2 produced by the PI4P5K SKTL controls apical size by tethering PAR-3 in Drosophila epithelial cells.

Claret S, Jouette J, Benoit B, Legent K, Guichet A.

Curr Biol. 2014 May 19;24(10):1071-9. doi: 10.1016/j.cub.2014.03.056. Epub 2014 Apr 24.

21.

New management strategy of pregnancies at risk of congenital adrenal hyperplasia using fetal sex determination in maternal serum: French cohort of 258 cases (2002-2011).

Tardy-Guidollet V, Menassa R, Costa JM, David M, Bouvattier-Morel C, Baumann C, Houang M, Lorenzini F, Philip N, Odent S, Guichet A, Morel Y.

J Clin Endocrinol Metab. 2014 Apr;99(4):1180-8. doi: 10.1210/jc.2013-2895. Epub 2014 Jan 28.

PMID:
24471566
22.

Fetal intracerebral hemorrhage and cataract: think COL4A1.

Colin E, Sentilhes L, Sarfati A, Mine M, Guichet A, Ploton C, Boussion F, Delorme B, Tournier-Lasserve E, Bonneau D.

J Perinatol. 2014 Jan;34(1):75-7. doi: 10.1038/jp.2013.135.

PMID:
24374867
23.

Establishment and mitotic characterization of new Drosophila acentriolar cell lines from DSas-4 mutant.

Lecland N, Debec A, Delmas A, Moutinho-Pereira S, Malmanche N, Bouissou A, Dupré C, Jourdan A, Raynaud-Messina B, Maiato H, Guichet A.

Biol Open. 2013 Mar 15;2(3):314-23. doi: 10.1242/bio.20133327. Epub 2013 Jan 17.

24.

Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia.

Ben Khelifa M, Coutton C, Blum MG, Abada F, Harbuz R, Zouari R, Guichet A, May-Panloup P, Mitchell V, Rollet J, Triki C, Merdassi G, Vialard F, Koscinski I, Viville S, Keskes L, Soulie JP, Rives N, Dorphin B, Lestrade F, Hesters L, Poirot C, Benzacken B, Jouk PS, Satre V, Hennebicq S, Arnoult C, Lunardi J, Ray PF.

Hum Reprod. 2012 Nov;27(11):3337-46. doi: 10.1093/humrep/des296. Epub 2012 Aug 11.

PMID:
22888167
25.

Drosophila tubulin-binding cofactor B is required for microtubule network formation and for cell polarity.

Baffet AD, Benoit B, Januschke J, Audo J, Gourhand V, Roth S, Guichet A.

Mol Biol Cell. 2012 Sep;23(18):3591-601. doi: 10.1091/mbc.E11-07-0633. Epub 2012 Aug 1.

26.

Prenatal diagnosis of CHARGE syndrome by identification of a novel CHD7 mutation in a previously unaffected family.

Colin E, Bonneau D, Boussion F, Guichet A, Delorme B, Triau S, Gillard P, Kitzis A, Bilan F.

Prenat Diagn. 2012 Jul;32(7):692-4. doi: 10.1002/pd.3876. Epub 2012 Apr 20.

PMID:
22517486
27.

Relationship of non-visualization of the fetal gallbladder and amniotic fluid digestive enzymes analysis to outcome.

Dreux S, Boughanim M, Lepinard C, Guichet A, Rival JM, de Becdelievre A, Dugueperoux I, Muller F.

Prenat Diagn. 2012 May;32(5):423-6. doi: 10.1002/pd.3830. Epub 2012 Apr 11.

PMID:
22495616
28.

Barth syndrome in a female patient.

Cosson L, Toutain A, Simard G, Kulik W, Matyas G, Guichet A, Blasco H, Maakaroun-Vermesse Z, Vaillant MC, Le Caignec C, Chantepie A, Labarthe F.

Mol Genet Metab. 2012 May;106(1):115-20. doi: 10.1016/j.ymgme.2012.01.015. Epub 2012 Jan 24.

PMID:
22410210
29.

Binder phenotype in mothers affected with autoimmune disorders.

Colin E, Touraine R, Levaillant JM, Pasquier L, Boussion F, Ferry M, Guichet A, Barth M, Mercier A, Gérard-Blanluet M, Odent S, Bonneau D.

J Matern Fetal Neonatal Med. 2012 Aug;25(8):1413-8. doi: 10.3109/14767058.2011.636105. Epub 2011 Dec 7.

PMID:
22082304
30.

Nucleoporin98-96 function is required for transit amplification divisions in the germ line of Drosophila melanogaster.

Parrott BB, Chiang Y, Hudson A, Sarkar A, Guichet A, Schulz C.

PLoS One. 2011;6(9):e25087. doi: 10.1371/journal.pone.0025087. Epub 2011 Sep 16.

31.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

Jacquemont S, Reymond A, Zufferey F, Harewood L, Walters RG, Kutalik Z, Martinet D, Shen Y, Valsesia A, Beckmann ND, Thorleifsson G, Belfiore M, Bouquillon S, Campion D, de Leeuw N, de Vries BB, Esko T, Fernandez BA, Fernández-Aranda F, Fernández-Real JM, Gratacòs M, Guilmatre A, Hoyer J, Jarvelin MR, Kooy RF, Kurg A, Le Caignec C, Männik K, Platt OS, Sanlaville D, Van Haelst MM, Villatoro Gomez S, Walha F, Wu BL, Yu Y, Aboura A, Addor MC, Alembik Y, Antonarakis SE, Arveiler B, Barth M, Bednarek N, Béna F, Bergmann S, Beri M, Bernardini L, Blaumeiser B, Bonneau D, Bottani A, Boute O, Brunner HG, Cailley D, Callier P, Chiesa J, Chrast J, Coin L, Coutton C, Cuisset JM, Cuvellier JC, David A, de Freminville B, Delobel B, Delrue MA, Demeer B, Descamps D, Didelot G, Dieterich K, Disciglio V, Doco-Fenzy M, Drunat S, Duban-Bedu B, Dubourg C, El-Sayed Moustafa JS, Elliott P, Faas BH, Faivre L, Faudet A, Fellmann F, Ferrarini A, Fisher R, Flori E, Forer L, Gaillard D, Gerard M, Gieger C, Gimelli S, Gimelli G, Grabe HJ, Guichet A, Guillin O, Hartikainen AL, Heron D, Hippolyte L, Holder M, Homuth G, Isidor B, Jaillard S, Jaros Z, Jiménez-Murcia S, Helas GJ, Jonveaux P, Kaksonen S, Keren B, Kloss-Brandstätter A, Knoers NV, Koolen DA, Kroisel PM, Kronenberg F, Labalme A, Landais E, Lapi E, Layet V, Legallic S, Leheup B, Leube B, Lewis S, Lucas J, MacDermot KD, Magnusson P, Marshall C, Mathieu-Dramard M, McCarthy MI, Meitinger T, Mencarelli MA, Merla G, Moerman A, Mooser V, Morice-Picard F, Mucciolo M, Nauck M, Ndiaye NC, Nordgren A, Pasquier L, Petit F, Pfundt R, Plessis G, Rajcan-Separovic E, Ramelli GP, Rauch A, Ravazzolo R, Reis A, Renieri A, Richart C, Ried JS, Rieubland C, Roberts W, Roetzer KM, Rooryck C, Rossi M, Saemundsen E, Satre V, Schurmann C, Sigurdsson E, Stavropoulos DJ, Stefansson H, Tengström C, Thorsteinsdóttir U, Tinahones FJ, Touraine R, Vallée L, van Binsbergen E, Van der Aa N, Vincent-Delorme C, Visvikis-Siest S, Vollenweider P, Völzke H, Vulto-van Silfhout AT, Waeber G, Wallgren-Pettersson C, Witwicki RM, Zwolinksi S, Andrieux J, Estivill X, Gusella JF, Gustafsson O, Metspalu A, Scherer SW, Stefansson K, Blakemore AI, Beckmann JS, Froguel P.

Nature. 2011 Aug 31;478(7367):97-102. doi: 10.1038/nature10406.

32.

A developmentally regulated two-step process generates a noncentrosomal microtubule network in Drosophila tracheal cells.

Brodu V, Baffet AD, Le Droguen PM, Casanova J, Guichet A.

Dev Cell. 2010 May 18;18(5):790-801. doi: 10.1016/j.devcel.2010.03.015.

33.

Phosphatidylinositol 4,5-bisphosphate directs spermatid cell polarity and exocyst localization in Drosophila.

Fabian L, Wei HC, Rollins J, Noguchi T, Blankenship JT, Bellamkonda K, Polevoy G, Gervais L, Guichet A, Fuller MT, Brill JA.

Mol Biol Cell. 2010 May 1;21(9):1546-55. doi: 10.1091/mbc.E09-07-0582. Epub 2010 Mar 17.

34.

Drosophila stathmins bind tubulin heterodimers with high and variable stoichiometries.

Lachkar S, Lebois M, Steinmetz MO, Guichet A, Lal N, Curmi PA, Sobel A, Ozon S.

J Biol Chem. 2010 Apr 9;285(15):11667-80. doi: 10.1074/jbc.M109.096727. Epub 2010 Feb 9.

35.

Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.

Jaillard S, Drunat S, Bendavid C, Aboura A, Etcheverry A, Journel H, Delahaye A, Pasquier L, Bonneau D, Toutain A, Burglen L, Guichet A, Pipiras E, Gilbert-Dussardier B, Benzacken B, Martin-Coignard D, Henry C, David A, Lucas J, Mosser J, David V, Odent S, Verloes A, Dubourg C.

Eur J Med Genet. 2010 Mar-Apr;53(2):66-75. doi: 10.1016/j.ejmg.2009.10.002. Epub 2009 Oct 28.

PMID:
19878743
36.

MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations.

Le Meur N, Holder-Espinasse M, Jaillard S, Goldenberg A, Joriot S, Amati-Bonneau P, Guichet A, Barth M, Charollais A, Journel H, Auvin S, Boucher C, Kerckaert JP, David V, Manouvrier-Hanu S, Saugier-Veber P, Frébourg T, Dubourg C, Andrieux J, Bonneau D.

J Med Genet. 2010 Jan;47(1):22-9. doi: 10.1136/jmg.2009.069732. Epub 2009 Jul 9.

37.

Interplay between Rab5 and PtdIns(4,5)P2 controls early endocytosis in the Drosophila germline.

Compagnon J, Gervais L, Roman MS, Chamot-Boeuf S, Guichet A.

J Cell Sci. 2009 Jan 1;122(Pt 1):25-35. doi: 10.1242/jcs.033027. Epub 2008 Dec 2.

38.

A dual role for actin and microtubule cytoskeleton in the transport of Golgi units from the nurse cells to the oocyte across ring canals.

Nicolas E, Chenouard N, Olivo-Marin JC, Guichet A.

Mol Biol Cell. 2009 Jan;20(1):556-68. doi: 10.1091/mbc.E08-04-0360. Epub 2008 Nov 12.

39.

PIP5K-dependent production of PIP2 sustains microtubule organization to establish polarized transport in the Drosophila oocyte.

Gervais L, Claret S, Januschke J, Roth S, Guichet A.

Development. 2008 Dec;135(23):3829-38. doi: 10.1242/dev.029009. Epub 2008 Oct 23. Erratum in: Development. 2008 Dec;135(23):3970.

40.

Influence of ultrasonographers training on prenatal diagnosis of congenital heart diseases: a 12-year population-based study.

Pézard P, Bonnemains L, Boussion F, Sentilhes L, Allory P, Lépinard C, Guichet A, Triau S, Biquard F, Leblanc M, Bonneau D, Descamps P.

Prenat Diagn. 2008 Nov;28(11):1016-22. doi: 10.1002/pd.2113.

PMID:
18925579
41.

Overexpression of partner of numb induces asymmetric distribution of the PI4P 5-Kinase Skittles in mitotic sensory organ precursor cells in Drosophila.

Perdigoto CN, Gervais L, Overstreet E, Fischer J, Guichet A, Schweisguth F.

PLoS One. 2008 Aug 27;3(8):e3072. doi: 10.1371/journal.pone.0003072.

42.

Increased aneuploidy rates in spermatozoa of a male carrier of a trisomy 18 mosaicism.

Perrin A, Douet-Guilbert N, Le Bris MJ, May-Panloup P, Guichet A, Amice V, Amice J, De Braekeleer M, Morel F.

Int J Androl. 2009 Jun;32(3):231-4. doi: 10.1111/j.1365-2605.2007.00840.x. Epub 2008 Jan 22.

PMID:
18217987
43.

Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia.

Schneider A, Benzacken B, Guichet A, Verloes A, Bonneau D, Collot N, Dastot-Le-Moal F, Goossens M, Taine L, Landais E, Gaillard D, Doco-Fenzy M.

Eur J Hum Genet. 2008 Jun;16(6):680-7. doi: 10.1038/sj.ejhg.5201977. Epub 2008 Jan 16.

44.

Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome.

Ricard-Mousnier B, N'Guyen S, Dubas F, Pouplard F, Guichet A.

Epileptic Disord. 2007 Sep;9(3):327-31. Epub 2007 Sep 20.

45.

Endocrine function in a 48,XXYY adult with type 2 diabetes: case report with a review of the literature.

Dubois S, Illouz F, Pinson L, Bonneau D, Rohmer V, Guichet A.

Ann Endocrinol (Paris). 2007 Oct;68(5):384-8. Epub 2007 Sep 11.

PMID:
17850758
46.

Rab6 and the secretory pathway affect oocyte polarity in Drosophila.

Januschke J, Nicolas E, Compagnon J, Formstecher E, Goud B, Guichet A.

Development. 2007 Oct;134(19):3419-25.

47.

Heterozygous mutation of steroidogenic factor-1 in 46,XY subjects may mimic partial androgen insensitivity syndrome.

Coutant R, Mallet D, Lahlou N, Bouhours-Nouet N, Guichet A, Coupris L, Croué A, Morel Y.

J Clin Endocrinol Metab. 2007 Aug;92(8):2868-73. Epub 2007 May 8.

PMID:
17488792
48.

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

Loiseau D, Chevrollier A, Verny C, Guillet V, Gueguen N, Pou de Crescenzo MA, Ferré M, Malinge MC, Guichet A, Nicolas G, Amati-Bonneau P, Malthièry Y, Bonneau D, Reynier P.

Ann Neurol. 2007 Apr;61(4):315-23.

PMID:
17444508
49.

Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis.

Olichon A, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Guichet A, Delettre C, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, Belenguer P.

J Cell Physiol. 2007 May;211(2):423-30.

PMID:
17167772
50.

The centrosome-nucleus complex and microtubule organization in the Drosophila oocyte.

Januschke J, Gervais L, Gillet L, Keryer G, Bornens M, Guichet A.

Development. 2006 Jan;133(1):129-39. Epub 2005 Nov 30.

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