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Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.
Genet Med. 2019 Aug;21(8):1897-1898. doi: 10.1038/s41436-018-0327-7.
Genet Med. 2019.
PMID: 30279470
Free PMC article.
IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.
Mignot C, McMahon AC, Bar C, Campeau PM, Davidson C, Buratti J, Nava C, Jacquemont ML, Tallot M, Milh M, Edery P, Marzin P, Barcia G, Barnerias C, Besmond C, Bienvenu T, Bruel AL, Brunga L, Ceulemans B, Coubes C, Cristancho AG, Cunningham F, Dehouck MB, Donner EJ, Duban-Bedu B, Dubourg C, Gardella E, Gauthier J, Geneviève D, Gobin-Limballe S, Goldberg EM, Hagebeuk E, Hamdan FF, Hančárová M, Hubert L, Ioos C, Ichikawa S, Janssens S, Journel H, Kaminska A, Keren B, Koopmans M, Lacoste C, Laššuthová P, Lederer D, Lehalle D, Marjanovic D, Métreau J, Michaud JL, Miller K, Minassian BA, Morales J, Moutard ML, Munnich A, Ortiz-Gonzalez XR, Pinard JM, Prchalová D, Putoux A, Quelin C, Rosen AR, Roume J, Rossignol E, Simon MEH, Smol T, Shur N, Shelihan I, Štěrbová K, Vyhnálková E, Vilain C, Soblet J, Smits G, Yang SP, van der Smagt JJ, van Hasselt PM, van Kempen M, Weckhuysen S, Helbig I, Villard L, Héron D, Koeleman B, Møller RS, Lesca G, Helbig KL, Nabbout R, Verbeek NE, Depienne C.
Mignot C, et al. Among authors: dehouck mb.
Genet Med. 2019 Apr;21(4):837-849. doi: 10.1038/s41436-018-0268-1. Epub 2018 Sep 12.
Genet Med. 2019.
PMID: 30206421
Free PMC article.
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Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay.
Andrieux J, Richebourg S, Duban-Bedu B, Petit F, Leprêtre F, Sukno S, Dehouck MB, Delobel B.
Andrieux J, et al. Among authors: dehouck mb.
Eur J Med Genet. 2008 Jul-Aug;51(4):373-81. doi: 10.1016/j.ejmg.2008.02.010. Epub 2008 Mar 28.
Eur J Med Genet. 2008.
PMID: 18463015
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The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability.
Vandewalle J, Bauters M, Van Esch H, Belet S, Verbeeck J, Fieremans N, Holvoet M, Vento J, Spreiz A, Kotzot D, Haberlandt E, Rosenfeld J, Andrieux J, Delobel B, Dehouck MB, Devriendt K, Fryns JP, Marynen P, Goldstein A, Froyen G.
Vandewalle J, et al. Among authors: dehouck mb.
Hum Genet. 2013 Oct;132(10):1177-85. doi: 10.1007/s00439-013-1322-3. Epub 2013 Jun 20.
Hum Genet. 2013.
PMID: 23783460
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[Cerebral agyria-pachygyria in a child with Werdnig-Hoffmann disease].
Cneude F, Sukno S, Boidein F, Dehouck MB, Bourlet A, Vittu G.
Cneude F, et al. Among authors: dehouck mb.
Rev Neurol (Paris). 1999 Sep;155(8):589-91.
Rev Neurol (Paris). 1999.
PMID: 10486849
French.
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[Fetal cerebral ventriculomegaly. Etiology and outcome, report of 141 cases].
Valat AS, Dehouck MB, Dufour P, Dubos JP, Djebara AE, Dewismes L, Robert Y, Puech F.
Valat AS, et al. Among authors: dehouck mb.
J Gynecol Obstet Biol Reprod (Paris). 1998 Dec;27(8):782-9.
J Gynecol Obstet Biol Reprod (Paris). 1998.
PMID: 10021991
Free article.
French.
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[Management of newborn life-threatening distress at birth. Study of the experience at a university maternity ward].
Dubos JP, Truffert P, Dehouck MB, Depoortere MH, Thomas D, Duvaux C, Valat AS, Lequien P, Puech F.
Dubos JP, et al. Among authors: dehouck mb.
J Gynecol Obstet Biol Reprod (Paris). 1994;23(3):330-5.
J Gynecol Obstet Biol Reprod (Paris). 1994.
PMID: 8051359
French.
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