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1987 | 1 |
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Page 1
Phenotypic spectrum of Simpson-Golabi-Behmel syndrome in a series of 42 cases with a mutation in GPC3 and review of the literature.
Am J Med Genet C Semin Med Genet. 2013 May;163C(2):92-105. doi: 10.1002/ajmg.c.31360. Epub 2013 Apr 18.
Am J Med Genet C Semin Med Genet. 2013.
PMID: 23606591
Review.
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.
Klein J, Buffin-Meyer B, Boizard F, Moussaoui N, Lescat O, Breuil B, Fedou C, Feuillet G, Casemayou A, Neau E, Hindryckx A, Decatte L, Levtchenko E, Raaijmakers A, Vayssière C, Goua V, Lucas C, Perrotin F, Cloarec S, Benachi A, Manca-Pellissier MC, Delmas HL, Bessenay L, Le Vaillant C, Allain-Launay E, Gondry J, Boudailliez B, Simon E, Prieur F, Lavocat MP, Saliou AH, De Parscau L, Bidat L, Noel C, Floch C, Bourdat-Michel G, Favre R, Weingertner AS, Oury JF, Baudouin V, Bory JP, Pietrement C, Fiorenza M, Massardier J, Kessler S, Lounis N, Auriol FC, Marcorelles P, Collardeau-Frachon S, Zürbig P, Mischak H, Magalhães P, Batut J, Blader P, Saulnier Blache JS, Bascands JL, Schaefer F, Decramer S, Schanstra JP; BIOMAN consortium.
Klein J, et al.
Kidney Int. 2021 Mar;99(3):737-749. doi: 10.1016/j.kint.2020.06.043. Epub 2020 Aug 1.
Kidney Int. 2021.
PMID: 32750455
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Use of parenteral lipid emulsions in French neonatal ICUs.
Lapillonne A, Fellous L, Kermorvant-Duchemin E; French neonatal departments.
Lapillonne A, et al.
Nutr Clin Pract. 2011 Dec;26(6):672-80. doi: 10.1177/0884533611425681.
Nutr Clin Pract. 2011.
PMID: 22205555
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The ANTENATAL multicentre study to predict postnatal renal outcome in fetuses with posterior urethral valves: objectives and design.
Buffin-Meyer B, Klein J, van der Zanden LFM, Levtchenko E, Moulos P, Lounis N, Conte-Auriol F, Hindryckx A, Wühl E, Persico N, Oepkes D, Schreuder MF, Tkaczyk M, Ariceta G, Fossum M, Parvex P, Feitz W, Olsen H, Montini G, Decramer S, Schanstra JP; ANTENATAL Consortium.
Buffin-Meyer B, et al.
Clin Kidney J. 2019 Sep 26;13(3):371-379. doi: 10.1093/ckj/sfz107. eCollection 2020 Jun.
Clin Kidney J. 2019.
PMID: 32699617
Free PMC article.
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Abnormal phenotype in a child with a "balanced" translocation 8/12 in mosaic state.
Saura R, Longy M, Serville F, Chokairi O, Froute MF.
Saura R, et al. Among authors: froute mf.
Am J Med Genet. 1987 Dec;28(4):1021-3. doi: 10.1002/ajmg.1320280432.
Am J Med Genet. 1987.
PMID: 3688015
No abstract available.
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