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Items: 1 to 50 of 212

1.

Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway.

Karolak JA, Vincent M, Deutsch G, Gambin T, Cogné B, Pichon O, Vetrini F, Mefford HC, Dines JN, Golden-Grant K, Dipple K, Freed AS, Leppig KA, Dishop M, Mowat D, Bennetts B, Gifford AJ, Weber MA, Lee AF, Boerkoel CF, Bartell TM, Ward-Melver C, Besnard T, Petit F, Bache I, Tümer Z, Denis-Musquer M, Joubert M, Martinovic J, Bénéteau C, Molin A, Carles D, André G, Bieth E, Chassaing N, Devisme L, Chalabreysse L, Pasquier L, Secq V, Don M, Orsaria M, Missirian C, Mortreux J, Sanlaville D, Pons L, Küry S, Bézieau S, Liet JM, Joram N, Bihouée T, Scott DA, Brown CW, Scaglia F, Tsai AC, Grange DK, Phillips JA 3rd, Pfotenhauer JP, Jhangiani SN, Gonzaga-Jauregui CG, Chung WK, Schauer GM, Lipson MH, Mercer CL, van Haeringen A, Liu Q, Popek E, Coban Akdemir ZH, Lupski JR, Szafranski P, Isidor B, Le Caignec C, Stankiewicz P.

Am J Hum Genet. 2019 Feb 7;104(2):213-228. doi: 10.1016/j.ajhg.2018.12.010. Epub 2019 Jan 10.

PMID:
30639323
2.

Fetal phenotype of Rubinstein-Taybi syndrome caused by CREBBP mutations.

Van-Gils J, Naudion S, Toutain J, Lancelot G, Attié-Bitach T, Blesson S, Demeer B, Doray B, Gonzales M, Martinovic J, Whalen S, Taine L, Arveiler B, Lacombe D, Fergelot P.

Clin Genet. 2019 Mar;95(3):420-426. doi: 10.1111/cge.13493. Epub 2019 Jan 11.

PMID:
30633342
3.

Bardet-Biedl syndrome: Antenatal presentation of forty-five fetuses with biallelic pathogenic variants in known Bardet-Biedl syndrome genes.

Mary L, Chennen K, Stoetzel C, Antin M, Leuvrey A, Nourisson E, Alanio-Detton E, Antal MC, Attié-Bitach T, Bouvagnet P, Bouvier R, Buenerd A, Clémenson A, Devisme L, Gasser B, Gilbert-Dussardier B, Guimiot F, Khau Van Kien P, Leroy B, Loget P, Martinovic J, Pelluard F, Perez MJ, Petit F, Pinson L, Rooryck-Thambo C, Poch O, Dollfus H, Schaefer E, Muller J.

Clin Genet. 2019 Mar;95(3):384-397. doi: 10.1111/cge.13500.

PMID:
30614526
4.

Loss of function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish.

Reilly ML, Stokman MF, Magry V, Jeanpierre C, Alves M, Paydar M, Hellinga J, Delous M, Pouly D, Failler M, Martinovic J, Loeuillet L, Leroy B, Tantau J, Roume J, Evans CG, Shan X, Filges I, Allingham JS, Kwok BH, Saunier S, Giles RH, Benmerah A.

Hum Mol Genet. 2018 Nov 1. doi: 10.1093/hmg/ddy381. [Epub ahead of print]

PMID:
30388224
5.

Symmetry perception for patterns defined by color and luminance.

Martinovic J, Jennings BJ, Makin ADJ, Bertamini M, Angelescu I.

J Vis. 2018 Aug 1;18(8):4. doi: 10.1167/18.8.4.

PMID:
30098176
6.

Neural mechanisms of divided feature-selective attention to colour.

Martinovic J, Wuerger SM, Hillyard SA, Müller MM, Andersen SK.

Neuroimage. 2018 Nov 1;181:670-682. doi: 10.1016/j.neuroimage.2018.07.033. Epub 2018 Jul 24.

PMID:
30048748
7.

Congenital diaphragmatic hernia has a better prognosis when associated with a hernia sac.

Bouchghoul H, Marty O, Fouquet V, Cordier AG, Senat MV, Saada J, Mokhtari M, Le Sache N, Martinovic J, Benachi A.

Prenat Diagn. 2018 Aug;38(9):638-644. doi: 10.1002/pd.5326. Epub 2018 Jul 11.

PMID:
29956346
8.

Fetal cerebral hemorrhage due to X-linked GATA1 gene mutation.

Bouchghoul H, Quelin C, Loget P, Encha-Razavi F, Senat MV, Maheut L, Galimand J, Collardeau-Frachon S, Da Costa L, Martinovic J.

Prenat Diagn. 2018 Sep;38(10):772-778. doi: 10.1002/pd.5320. Epub 2018 Jul 24.

PMID:
29949202
9.

Discriminant analysis of cardiovascular and respiratory variables for classification of road cyclists by specialty.

Nikolić B, Martinović J, Matić M, Stefanović Đ.

J Sports Med Phys Fitness. 2018 May 29. doi: 10.23736/S0022-4707.18.08478-5. [Epub ahead of print]

PMID:
29845839
10.

Cortical summation and attentional modulation of combined chromatic and luminance signals.

Martinovic J, Andersen SK.

Neuroimage. 2018 Aug 1;176:390-403. doi: 10.1016/j.neuroimage.2018.04.066. Epub 2018 May 4.

PMID:
29730493
11.

Regional-specific effects of cerebral ischemia/reperfusion and dehydroepiandrosterone on synaptic NMDAR/PSD-95 complex in male Wistar rats.

Zaric M, Drakulic D, Stojanovic IG, Mitrovic N, Grkovic I, Martinovic J.

Brain Res. 2018 Jun 1;1688:73-80. doi: 10.1016/j.brainres.2018.03.023. Epub 2018 Mar 22.

PMID:
29577884
12.

Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigation.

Sudrié-Arnaud B, Marguet F, Patrier S, Martinovic J, Louillet F, Broux F, Charbonnier F, Dranguet H, Coutant S, Vezain M, Lanos R, Tebani A, Fuller M, Lamari F, Chambon P, Brehin AC, Trestard L, Tournier I, Marret S, Verspyck E, Laquerrière A, Bekri S.

Clin Chim Acta. 2018 Jun;481:1-8. doi: 10.1016/j.cca.2018.02.023. Epub 2018 Feb 22.

PMID:
29476731
13.

Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation.

Vivanti A, Ozanne A, Grondin C, Saliou G, Quevarec L, Maurey H, Aubourg P, Benachi A, Gut M, Gut I, Martinovic J, Sénat MV, Tawk M, Melki J.

Brain. 2018 Apr 1;141(4):979-988. doi: 10.1093/brain/awy020.

PMID:
29444212
14.

First prenatal case of proximal 19p13.12 microdeletion syndrome: New insights and new delineation of the syndrome.

Huynh MT, Tosca L, Petit F, Martinovic J, Proust A, Bouligand J, Amiel J, Azria E, Parisot F, Benoit V, Receveur A, Drévillon L, Tachdjian G, Brisset S.

Eur J Med Genet. 2018 Jun;61(6):322-328. doi: 10.1016/j.ejmg.2018.01.009. Epub 2018 Feb 3.

PMID:
29366875
15.

A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern.

Chartier S, Alby C, Boutaud L, Thomas S, Elkhartoufi N, Martinovic J, Kaplan J, Benachi A, Lacombe D, Sonigo P, Drunat S, Vekemans M, Agenor J, Encha Razavi F, Attie-Bitach T.

Birth Defects Res. 2018 Apr 17;110(7):598-602. doi: 10.1002/bdr2.1204. Epub 2018 Jan 22.

PMID:
29356416
16.

Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.

De Tomasi L, David P, Humbert C, Silbermann F, Arrondel C, Tores F, Fouquet S, Desgrange A, Niel O, Bole-Feysot C, Nitschké P, Roume J, Cordier MP, Pietrement C, Isidor B, Khau Van Kien P, Gonzales M, Saint-Frison MH, Martinovic J, Novo R, Piard J, Cabrol C, Verma IC, Puri R, Journel H, Aziza J, Gavard L, Said-Menthon MH, Heidet L, Saunier S, Jeanpierre C.

Am J Hum Genet. 2017 Nov 2;101(5):803-814. doi: 10.1016/j.ajhg.2017.09.026.

17.

Prenatal diagnosis of isochromosome 20q in a fetus with vertebral anomaly and rocker-bottom feet.

Receveur A, Brisset S, Martinovic J, Bazin A, Lhomann L, Colmant C, Pineau D, Gautier V, Tosca L, Tachdjian G.

Taiwan J Obstet Gynecol. 2017 Oct;56(5):677-680. doi: 10.1016/j.tjog.2017.08.018.

18.

Detailed muscular structure and neural control anatomy of the levator ani muscle: a study based on female human fetuses.

Nyangoh Timoh K, Moszkowicz D, Zaitouna M, Lebacle C, Martinovic J, Diallo D, Creze M, Lavoue V, Darai E, Benoit G, Bessede T.

Am J Obstet Gynecol. 2018 Jan;218(1):121.e1-121.e12. doi: 10.1016/j.ajog.2017.09.021. Epub 2017 Oct 6.

PMID:
28988909
19.

WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.

Cavallin M, Rujano MA, Bednarek N, Medina-Cano D, Bernabe Gelot A, Drunat S, Maillard C, Garfa-Traore M, Bole C, Nitschké P, Beneteau C, Besnard T, Cogné B, Eveillard M, Kuster A, Poirier K, Verloes A, Martinovic J, Bidat L, Rio M, Lyonnet S, Reilly ML, Boddaert N, Jenneson-Liver M, Motte J, Doco-Fenzy M, Chelly J, Attie-Bitach T, Simons M, Cantagrel V, Passemard S, Baffet A, Thomas S, Bahi-Buisson N.

Brain. 2017 Oct 1;140(10):2597-2609. doi: 10.1093/brain/awx218.

PMID:
28969387
20.

TIMP-3 mRNA expression levels positively correlates with levels of miR-21 in in situ BC and negatively in PR positive invasive BC.

Petrovic N, Sami A, Martinovic J, Zaric M, Nakashidze I, Lukic S, Jovanovic-Cupic S.

Pathol Res Pract. 2017 Oct;213(10):1264-1270. doi: 10.1016/j.prp.2017.08.012. Epub 2017 Sep 6.

PMID:
28935174
21.

Fetal Cerebral Ventricular Dilatation: Etiopathogenic Study of 130 Observations.

Darouich S, Boutaud L, Bessières B, Bonnière M, Martinovic J, Mechler C, Alby C, Bernard JP, Roth P, Ville Y, Malan V, Vekemans M, Attié-Bitach T, Encha-Razavi F.

Birth Defects Res. 2017 Nov 15;109(19):1586-1595. doi: 10.1002/bdr2.1093. Epub 2017 Jul 31.

PMID:
28758373
22.

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.

Heidet L, Morinière V, Henry C, De Tomasi L, Reilly ML, Humbert C, Alibeu O, Fourrage C, Bole-Feysot C, Nitschké P, Tores F, Bras M, Jeanpierre M, Pietrement C, Gaillard D, Gonzales M, Novo R, Schaefer E, Roume J, Martinovic J, Malan V, Salomon R, Saunier S, Antignac C, Jeanpierre C.

J Am Soc Nephrol. 2017 Oct;28(10):2901-2914. doi: 10.1681/ASN.2017010043. Epub 2017 May 31.

23.

Role of Ectonucleotidases in Synapse Formation During Brain Development: Physiological and Pathological Implications.

Grković I, Drakulić D, Martinović J, Mitrović N.

Curr Neuropharmacol. 2019;17(1):84-98. doi: 10.2174/1570159X15666170518151541.

PMID:
28521702
24.

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly.

Naud ME, Tosca L, Martinovic J, Saada J, Métay C, Drévillon L, Benoit V, Brisset S, Tachdjian G.

Case Rep Genet. 2017;2017:7803136. doi: 10.1155/2017/7803136. Epub 2017 Mar 29.

25.

Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing.

Kuentz P, St-Onge J, Duffourd Y, Courcet JB, Carmignac V, Jouan T, Sorlin A, Abasq-Thomas C, Albuisson J, Amiel J, Amram D, Arpin S, Attie-Bitach T, Bahi-Buisson N, Barbarot S, Baujat G, Bessis D, Boccara O, Bonnière M, Boute O, Bursztejn AC, Chiaverini C, Cormier-Daire V, Coubes C, Delobel B, Edery P, Chehadeh SE, Francannet C, Geneviève D, Goldenberg A, Haye D, Isidor B, Jacquemont ML, Khau Van Kien P, Lacombe D, Martin L, Martinovic J, Maruani A, Mathieu-Dramard M, Mazereeuw-Hautier J, Michot C, Mignot C, Miquel J, Morice-Picard F, Petit F, Phan A, Rossi M, Touraine R, Verloes A, Vincent M, Vincent-Delorme C, Whalen S, Willems M, Marle N, Lehalle D, Thevenon J, Thauvin-Robinet C, Hadj-Rabia S, Faivre L, Vabres P, Rivière JB.

Genet Med. 2017 Sep;19(9):989-997. doi: 10.1038/gim.2016.220. Epub 2017 Feb 2.

PMID:
28151489
26.

Pseudofeeders on fetal magnetic resonance imaging predict outcome in vein of Galen malformations.

Saliou G, Vraka I, Teglas JP, Senat MV, Durand P, Colmant C, Ozanne A, Martinovic J, Tissiere P, Adamsbaum C.

Ann Neurol. 2017 Feb;81(2):278-286. doi: 10.1002/ana.24873. Erratum in: Ann Neurol. 2017 Jun;81(6):912.

PMID:
28076893
27.

No correlation between mtDNA amount and methylation levels at the CpG island of POLG exon 2 in wild-type and mutant human differentiated cells.

Steffann J, Pouliet A, Adjal H, Bole C, Fourrage C, Martinovic J, Rolland-Galmiche L, Rotig A, Tores F, Munnich A, Bonnefont JP.

J Med Genet. 2017 May;54(5):324-329. doi: 10.1136/jmedgenet-2016-104335. Epub 2017 Jan 9.

PMID:
28069933
28.

Erratum to: 17β-Estradiol-Induced Synaptic Rearrangements Are Accompanied by Altered Ectonucleotidase Activities in Male Rat Hippocampal Synaptosomes.

Mitrović N, Zarić M, Drakulić D, Martinović J, Sévigny J, Stanojlović M, Nedeljković N, Grković I.

J Mol Neurosci. 2017 Mar;61(3):423-424. doi: 10.1007/s12031-016-0879-4. No abstract available.

PMID:
28035555
29.

17β-Estradiol-Induced Synaptic Rearrangements Are Accompanied by Altered Ectonucleotidase Activities in Male Rat Hippocampal Synaptosomes.

Mitrović N, Zarić M, Drakulić D, Martinović J, Sévigny J, Stanojlović M, Nedeljković N, Grković I.

J Mol Neurosci. 2017 Mar;61(3):412-422. doi: 10.1007/s12031-016-0877-6. Epub 2016 Dec 15. Erratum in: J Mol Neurosci. 2017 Mar;61(3):423-424.

PMID:
27981418
30.

Modulation of microsaccades by spatial frequency during object categorization.

Craddock M, Oppermann F, Müller MM, Martinovic J.

Vision Res. 2017 Jan;130:48-56. doi: 10.1016/j.visres.2016.10.011. Epub 2016 Dec 1.

31.

Levator ani muscle innervation: Anatomical study in human fetus.

Nyangoh Timoh K, Bessede T, Lebacle C, Zaitouna M, Martinovic J, Diallo D, Creze M, Chevallier JM, Darai E, Benoît G, Moszkowicz D.

Neurourol Urodyn. 2017 Aug;36(6):1464-1471. doi: 10.1002/nau.23145. Epub 2016 Nov 4.

PMID:
27813139
32.

Think of the Conus Medullaris at the Time of Diagnosis of Fetal Sacral Agenesis.

Mottet N, Martinovic J, Baeza C, Guimiot F, Bault JP, Aubry MC, Riethmuller D, Zerah M, Cretolle C, Benachi A.

Fetal Diagn Ther. 2017;42(2):137-143. doi: 10.1159/000451080. Epub 2016 Oct 29.

PMID:
27794580
33.

Lipid peroxidation as risk factor for endothelial dysfunction in antiphospholipid syndrome patients.

Stanisavljevic N, Stojanovich L, Marisavljevic D, Djokovic A, Dopsaj V, Kotur-Stevuljevic J, Martinovic J, Memon L, Radovanovic S, Todic B, Lisulov D.

Clin Rheumatol. 2016 Oct;35(10):2485-93. doi: 10.1007/s10067-016-3369-8. Epub 2016 Aug 25.

PMID:
27562033
34.

Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development.

Grković I, Bjelobaba I, Mitrović N, Lavrnja I, Drakulić D, Martinović J, Stanojlović M, Horvat A, Nedeljković N.

J Chem Neuroanat. 2016 Nov;77:10-18. doi: 10.1016/j.jchemneu.2016.04.001. Epub 2016 Apr 2.

PMID:
27049676
35.

Methylmalonic acid and neutrophil morphometric index in laboratory diagnosis of cobalamin deficiency without macrocytosis.

Totoskovic D, Dopsaj V, Martinovic J.

Int J Lab Hematol. 2016 Jun;38(3):265-72. doi: 10.1111/ijlh.12479. Epub 2016 Mar 19.

PMID:
26992463
36.

17β-Estradiol upregulates ecto-5'-nucleotidase (CD73) in hippocampal synaptosomes of female rats through action mediated by estrogen receptor-α and -β.

Mitrović N, Zarić M, Drakulić D, Martinović J, Stanojlović M, Sévigny J, Horvat A, Nedeljković N, Grković I.

Neuroscience. 2016 Jun 2;324:286-96. doi: 10.1016/j.neuroscience.2016.03.022. Epub 2016 Mar 14.

PMID:
26987957
37.

Confined blood chimerism in a monochorionic dizygotic sex discordant twin pregnancy conceived after induced ovulation.

Mayeur Le Bras A, Petit F, Benachi A, Bedel B, Oucherif S, Martinovic J, Armanet N, Tosca L, Gautier V, Parisot F, Labrune P, Tachdjian G, Brisset S.

Birth Defects Res A Clin Mol Teratol. 2016 Apr;106(4):298-303. doi: 10.1002/bdra.23457. Epub 2016 Mar 2.

PMID:
26931099
38.

Combining S-cone and luminance signals adversely affects discrimination of objects within backgrounds.

Jennings BJ, Tsattalios K, Chakravarthi R, Martinovic J.

Sci Rep. 2016 Feb 9;6:20504. doi: 10.1038/srep20504.

39.

A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome.

Nizon M, Henry M, Michot C, Baumann C, Bazin A, Bessières B, Blesson S, Cordier-Alex MP, David A, Delahaye-Duriez A, Delezoïde AL, Dieux-Coeslier A, Doco-Fenzy M, Faivre L, Goldenberg A, Layet V, Loget P, Marlin S, Martinovic J, Odent S, Pasquier L, Plessis G, Prieur F, Putoux A, Rio M, Testard H, Bonnefont JP, Cormier-Daire V.

Clin Genet. 2016 May;89(5):584-9. doi: 10.1111/cge.12720. Epub 2016 Feb 3.

40.

Increased TGF-β: a drawback of tracheal occlusion in human and experimental congenital diaphragmatic hernia?

Vuckovic A, Herber-Jonat S, Flemmer AW, Ruehl IM, Votino C, Segers V, Benachi A, Martinovic J, Nowakowska D, Dzieniecka M, Jani JC.

Am J Physiol Lung Cell Mol Physiol. 2016 Feb 15;310(4):L311-27. doi: 10.1152/ajplung.00122.2015. Epub 2015 Dec 4.

41.

Accounting for microsaccadic artifacts in the EEG using independent component analysis and beamforming.

Craddock M, Martinovic J, Müller MM.

Psychophysiology. 2016 Apr;53(4):553-65. doi: 10.1111/psyp.12593. Epub 2015 Dec 4.

42.

The expanding spectrum of COL2A1 gene variants IN 136 patients with a skeletal dysplasia phenotype.

Barat-Houari M, Dumont B, Fabre A, Them FT, Alembik Y, Alessandri JL, Amiel J, Audebert S, Baumann-Morel C, Blanchet P, Bieth E, Brechard M, Busa T, Calvas P, Capri Y, Cartault F, Chassaing N, Ciorca V, Coubes C, David A, Delezoide AL, Dupin-Deguine D, El Chehadeh S, Faivre L, Giuliano F, Goldenberg A, Isidor B, Jacquemont ML, Julia S, Kaplan J, Lacombe D, Lebrun M, Marlin S, Martin-Coignard D, Martinovic J, Masurel A, Melki J, Mozelle-Nivoix M, Nguyen K, Odent S, Philip N, Pinson L, Plessis G, Quélin C, Shaeffer E, Sigaudy S, Thauvin C, Till M, Touraine R, Vigneron J, Baujat G, Cormier-Daire V, Le Merrer M, Geneviève D, Touitou I.

Eur J Hum Genet. 2016 Jul;24(7):992-1000. doi: 10.1038/ejhg.2015.250. Epub 2015 Dec 2.

43.
44.

Association of Socioeconomic Factors and Sedentary Lifestyle in Belgrade's Suburb, Working Class Community.

Konevic S, Martinovic J, Djonovic N.

Iran J Public Health. 2015 Aug;44(8):1053-60.

45.

Dissection anatomique assistée par ordinateur (DAAO) du plexus rénal pour affiner la dénervation rénale dans le traitement de l'hypertension artérielle réfractaire.

Lebacle C, Nyangoh Timoh K, Martinovic J, Zaitouna M, Diallo D, Benoit G, Bessede T.

Prog Urol. 2015 Nov;25(13):818-9. doi: 10.1016/j.purol.2015.08.208. French. No abstract available.

PMID:
26544403
46.

Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.

Zillhardt JL, Poirier K, Broix L, Lebrun N, Elmorjani A, Martinovic J, Saillour Y, Muraca G, Nectoux J, Bessieres B, Fallet-Bianco C, Lyonnet S, Dulac O, Odent S, Rejeb I, Ben Jemaa L, Rivier F, Pinson L, Geneviève D, Musizzano Y, Bigi N, Leboucq N, Giuliano F, Philip N, Vilain C, Van Bogaert P, Maurey H, Beldjord C, Artiguenave F, Boland A, Olaso R, Masson C, Nitschké P, Deleuze JF, Bahi-Buisson N, Chelly J.

Eur J Hum Genet. 2016 Apr;24(4):611-4. doi: 10.1038/ejhg.2015.192. Epub 2015 Sep 23.

47.

Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts.

Raymond L, Francou B, Petit F, Tosca L, Briand-Suleau A, Metay C, Martinovic J, Cordier AG, Benachi A, Pineau D, Guiochon-Mantel A, Goossens M, Tachdjian G, Brisset S.

Eur J Med Genet. 2015 Nov;58(11):591-6. doi: 10.1016/j.ejmg.2015.09.006. Epub 2015 Sep 16.

PMID:
26386246
48.

Rare ACTG1 variants in fetal microlissencephaly.

Poirier K, Martinovic J, Laquerrière A, Cavallin M, Fallet-Bianco C, Desguerre I, Valence S, Grande-Goburghun J, Francannet C, Deleuze JF, Boland A, Chelly J, Bahi-Buisson N.

Eur J Med Genet. 2015 Aug;58(8):416-8. doi: 10.1016/j.ejmg.2015.06.006. Epub 2015 Jul 16.

PMID:
26188271
49.

Early and late effects of objecthood and spatial frequency on event-related potentials and gamma band activity.

Craddock M, Martinovic J, Müller MM.

BMC Neurosci. 2015 Feb 26;16:6. doi: 10.1186/s12868-015-0144-8.

50.

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

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