These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 32765936)

  • 41. Antisocial behaviour and lying: a neuropsychiatric presentation of agenesis of the corpus callosum.
    Roxanas MG; Massey JS; Chaganti J
    Australas Psychiatry; 2014 Oct; 22(5):461-6. PubMed ID: 25147316
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Familial agenesis of the corpus callosum: a new form].
    Castro-Gago M; Rodriguez-Nuñez A; Eiris J; Peña J; Tojo R; Novo-Rodriguez I
    Arch Fr Pediatr; 1993 Apr; 50(4):327-30. PubMed ID: 8379821
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Genetic heterogeneity in corpus callosum agenesis.
    Pânzaru MC; Popa S; Lupu A; Gavrilovici C; Lupu VV; Gorduza EV
    Front Genet; 2022; 13():958570. PubMed ID: 36246626
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Spectrum of corpus callosum agenesis.
    Sztriha L
    Pediatr Neurol; 2005 Feb; 32(2):94-101. PubMed ID: 15664768
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prognostic indicators in the prenatal diagnosis of agenesis of corpus callosum.
    Vergani P; Ghidini A; Strobelt N; Locatelli A; Mariani S; Bertalero C; Cavallone M
    Am J Obstet Gynecol; 1994 Mar; 170(3):753-8. PubMed ID: 8141196
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Agenesis and dysgenesis of the corpus callosum: clinical, genetic and neuroimaging findings in a series of 41 patients.
    Schell-Apacik CC; Wagner K; Bihler M; Ertl-Wagner B; Heinrich U; Klopocki E; Kalscheuer VM; Muenke M; von Voss H
    Am J Med Genet A; 2008 Oct; 146A(19):2501-11. PubMed ID: 18792984
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A familial Sonic Hedgehog (SHH) stop-gain mutation associated with agenesis of the corpus callosum, mild intellectual disability and facial dysmorphism.
    Yi X; Yuan X; Xie H; Chen X; Zhu Y
    Brain Dev; 2020 Nov; 42(10):771-774. PubMed ID: 32703609
    [TBL] [Abstract][Full Text] [Related]  

  • 48. KCC3 deficiency-induced disruption of paranodal loops and impairment of axonal excitability in the peripheral nervous system.
    Sun YT; Tzeng SF; Lin TS; Hsu KS; Delpire E; Shen MR
    Neuroscience; 2016 Oct; 335():91-102. PubMed ID: 27568057
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A novel heterozygous loss-of-function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature.
    Sagi-Dain L; Kurolap A; Ilivitzki A; Mory A; Paperna T; ; Kedar R; Gonzaga-Jauregui C; Peleg A; Baris Feldman H
    Am J Med Genet A; 2020 Jan; 182(1):205-212. PubMed ID: 31697046
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizures.
    Platzer K; Hüning I; Obieglo C; Schwarzmayr T; Gabriel R; Strom TM; Gillessen-Kaesbach G; Kaiser FJ
    Am J Med Genet A; 2014 Aug; 164A(8):1976-80. PubMed ID: 24798461
    [TBL] [Abstract][Full Text] [Related]  

  • 51. X-linked partial corpus callosum agenesis with mild intellectual disability: identification of a novel L1CAM pathogenic variant.
    Bousquet I; Bozon M; Castellani V; Touraine R; Piton A; Gérard B; Guibaud L; Sanlaville D; Edery P; Saugier-Veber P; Putoux A
    Neurogenetics; 2021 Mar; 22(1):43-51. PubMed ID: 33415589
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Whole-Exome Sequencing Revealed Mutations of
    Jiang Y; Qian YQ; Yang MM; Zhan QT; Chen Y; Xi FF; Sagnelli M; Dong MY; Zhao BH; Luo Q
    Front Genet; 2019; 10():1201. PubMed ID: 31824579
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder.
    Meyer J; Johannssen K; Freitag CM; Schraut K; Teuber I; Hahner A; Mainhardt C; Mössner R; Volz HP; Wienker TF; McKeane D; Stephan DA; Rouleau G; Reif A; Lesch KP
    Int J Neuropsychopharmacol; 2005 Dec; 8(4):495-504. PubMed ID: 16098236
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Agenesis of the corpus callosum in a premature infant associated with Langdon-Down syndrome].
    Velisavljev-Filipović G
    Med Pregl; 2005; 58(11-12):587-91. PubMed ID: 16673864
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Clinicopathological findings associated with agenesis of the corpus callosum.
    Jeret JS; Serur D; Wisniewski KE; Lubin RA
    Brain Dev; 1987; 9(3):255-64. PubMed ID: 3310713
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Agenesis of the corpus callosum in Turner syndrome with ring X.
    Abd SE; Wilson L; Howlin P; Patton MA; Wintgens AM; Wilson R
    Dev Med Child Neurol; 1997 Feb; 39(2):119-24. PubMed ID: 9062427
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Whole-exome sequencing reveals novel
    Lenberg JL; Pretorius DH; Rupe ES; Jones MC; Ramos GA; Andreasen TS
    Clin Case Rep; 2019 Apr; 7(4):656-660. PubMed ID: 30997057
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Novel de novo SPOCK1 mutation in a proband with developmental delay, microcephaly and agenesis of corpus callosum.
    Dhamija R; Graham JM; Smaoui N; Thorland E; Kirmani S
    Eur J Med Genet; 2014 Mar; 57(4):181-4. PubMed ID: 24583203
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Exome sequencing study of partial agenesis of the corpus callosum in men with developmental delay, epilepsy, and microcephaly.
    Meloche J; Brunet V; Gagnon PA; Lavoie MÈ; Bouchard JB; Nadaf J; Majewski J; Morin C; Laprise C
    Mol Genet Genomic Med; 2020 Jan; 8(1):e992. PubMed ID: 31578829
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Morphometric variability of neuroimaging features in children with agenesis of the corpus callosum.
    Neal JB; Filippi CG; Mayeux R
    BMC Neurol; 2015 Jul; 15():116. PubMed ID: 26209096
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.