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 *

142 related articles for article (PubMed ID: 30205212)

  • 21. Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement.
    Su J; Lu W; Li M; Zhang Q; Chen F; Yi S; Yang Q; Yi S; Zhou X; Huang L; Shen Y; Luo J; Qin Z
    Mol Genet Genomic Med; 2021 Apr; 9(4):e1624. PubMed ID: 33724704
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel mutation in L1CAM gene in a Japanese patient with X-linked hydrocephalus.
    Okamoto N; Wada Y; Kawabata H; Ishikiriyama S; Takahashi S
    Jpn J Hum Genet; 1996 Dec; 41(4):431-7. PubMed ID: 9088116
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Strain-specific differences in brain gene expression in a hydrocephalic mouse model with motile cilia dysfunction.
    McKenzie CW; Preston CC; Finn R; Eyster KM; Faustino RS; Lee L
    Sci Rep; 2018 Sep; 8(1):13370. PubMed ID: 30190587
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.
    Jin SC; Dong W; Kundishora AJ; Panchagnula S; Moreno-De-Luca A; Furey CG; Allocco AA; Walker RL; Nelson-Williams C; Smith H; Dunbar A; Conine S; Lu Q; Zeng X; Sierant MC; Knight JR; Sullivan W; Duy PQ; DeSpenza T; Reeves BC; Karimy JK; Marlier A; Castaldi C; Tikhonova IR; Li B; Peña HP; Broach JR; Kabachelor EM; Ssenyonga P; Hehnly C; Ge L; Keren B; Timberlake AT; Goto J; Mangano FT; Johnston JM; Butler WE; Warf BC; Smith ER; Schiff SJ; Limbrick DD; Heuer G; Jackson EM; Iskandar BJ; Mane S; Haider S; Guclu B; Bayri Y; Sahin Y; Duncan CC; Apuzzo MLJ; DiLuna ML; Hoffman EJ; Sestan N; Ment LR; Alper SL; Bilguvar K; Geschwind DH; Günel M; Lifton RP; Kahle KT
    Nat Med; 2020 Nov; 26(11):1754-1765. PubMed ID: 33077954
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A recurrent de novo missense pathogenic variant in SMARCB1 causes severe intellectual disability and choroid plexus hyperplasia with resultant hydrocephalus.
    Diets IJ; Prescott T; Champaigne NL; Mancini GMS; Krossnes B; Frič R; Kocsis K; Jongmans MCJ; Kleefstra T
    Genet Med; 2019 Mar; 21(3):572-579. PubMed ID: 29907796
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The syndrome of sex-linked hydrocephalus.
    EDWARDS JH
    Arch Dis Child; 1961 Oct; 36(189):486-93. PubMed ID: 13889295
    [No Abstract]   [Full Text] [Related]  

  • 27. Sex-linked hydrocephalus. Report of a family with 15 affected members.
    EDWARDS JH; NORMAN RM; ROBERTS JM
    Arch Dis Child; 1961 Oct; 36(189):481-5. PubMed ID: 13889294
    [No Abstract]   [Full Text] [Related]  

  • 28. The Lhx9 homeobox gene controls pineal gland development and prevents postnatal hydrocephalus.
    Yamazaki F; Møller M; Fu C; Clokie SJ; Zykovich A; Coon SL; Klein DC; Rath MF
    Brain Struct Funct; 2015; 220(3):1497-509. PubMed ID: 24647753
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Congenital hydrocephalus in clinical practice: a genetic diagnostic approach.
    Verhagen JM; Schrander-Stumpel CT; Krapels IP; de Die-Smulders CE; van Lint FH; Willekes C; Weber JW; Gavilanes AW; Macville MV; Stegmann AP; Engelen JJ; Bakker J; Vos YJ; Frints SG
    Eur J Med Genet; 2011; 54(6):e542-7. PubMed ID: 21839187
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The family history of uncomplicated congenital hydrocephalus: an epidemiological study based on 270 probands.
    Lorber J
    Br Med J (Clin Res Ed); 1984 Aug; 289(6440):281-4. PubMed ID: 6430438
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital hydrocephalus and clasped thumbs: two cases of brothers in a family.
    Mochizuki Y; Suyehiro Y; Ihara Y; Tomimoto K; Saito A; Ito T
    Brain Dev; 1981; 3(4):407-9. PubMed ID: 7316097
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital genetic murine (ch) hydrocephalus. A structural model of cellular dysplasia and disorganization with the molecular locus of deficient proteoglycan synthesis.
    Richardson RR
    Childs Nerv Syst; 1985; 1(2):87-99. PubMed ID: 3924403
    [TBL] [Abstract][Full Text] [Related]  

  • 33. First reports of fetal SMARCC1 related hydrocephalus.
    Rive Le Gouard N; Nicolle R; Lefebvre M; Gelot A; Heide S; Gerasimenko A; Grigorescu R; Derive N; Jouannic JM; Garel C; Valence S; Quenum-Miraillet G; Chantot-Bastaraud S; Keren B; Heron D; Attie-Bitach T
    Eur J Med Genet; 2023 Aug; 66(8):104797. PubMed ID: 37285932
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Impaired methylation modifications of FZD3 alter chromatin accessibility and are involved in congenital hydrocephalus pathogenesis.
    Wang L; Shangguan S; Chang S; Wang Z; Lu X; Wu L; Li R; Bao Y; Qiu Z; Niu B; Zhang T
    Brain Res; 2014 Jun; 1569():48-56. PubMed ID: 24796881
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital hydrocephalus and cerebellar agenesis.
    Riccardi VM; Marcus ES
    Clin Genet; 1978 May; 13(5):443-7. PubMed ID: 657584
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [The etiology of congenital hydrocephalus with regard to a case of concordant hydrocephalus in monozygotic twins].
    BORLE A
    J Genet Hum; 1953 Dec; 2(3-4):157-202. PubMed ID: 13152349
    [No Abstract]   [Full Text] [Related]  

  • 37. Catamnestic investigations in children with congenital hydrocephalus.
    Angerpointner TA; Pockrandt L; Schroer K
    Z Kinderchir; 1990 Jun; 45(3):151-5. PubMed ID: 2375184
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Family study of congenital hydrocephalus.
    Adams C; Johnston WP; Nevin NC
    Dev Med Child Neurol; 1982 Aug; 24(4):493-8. PubMed ID: 6749581
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Surprisingly good outcome in antenatal diagnosis of severe hydrocephalus related to CCDC88C deficiency.
    Wallis M; Baumer A; Smaili W; Jaouad IC; Sefiani A; Jacobson E; Bowyer L; Mowat D; Rauch A
    Eur J Med Genet; 2018 Apr; 61(4):189-196. PubMed ID: 29225145
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Graded phenotypic response to partial and complete deficiency of a brain-specific transcript variant of the winged helix transcription factor RFX4.
    Blackshear PJ; Graves JP; Stumpo DJ; Cobos I; Rubenstein JL; Zeldin DC
    Development; 2003 Oct; 130(19):4539-52. PubMed ID: 12925582
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.