BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

253 related articles for article (PubMed ID: 31297068)

  • 1. The Many Faces of
    Lasser M; Pratt B; Monahan C; Kim SW; Lowery LA
    Front Physiol; 2019; 10():817. PubMed ID: 31297068
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in
    Mills A; Bearce E; Cella R; Kim SW; Selig M; Lee S; Lowery LA
    Front Physiol; 2019; 10():431. PubMed ID: 31031646
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exploring the developmental mechanisms underlying Wolf-Hirschhorn Syndrome: Evidence for defects in neural crest cell migration.
    Rutherford EL; Lowery LA
    Dev Biol; 2016 Dec; 420(1):1-10. PubMed ID: 27777068
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiple congenital malformations of Wolf-Hirschhorn syndrome are recapitulated in Fgfrl1 null mice.
    Catela C; Bilbao-Cortes D; Slonimsky E; Kratsios P; Rosenthal N; Te Welscher P
    Dis Model Mech; 2009; 2(5-6):283-94. PubMed ID: 19383940
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Corrigendum: Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in
    Mills A; Bearce E; Cella R; Kim SW; Selig M; Lee S; Lowery LA
    Front Physiol; 2020; 11():644596. PubMed ID: 33664672
    [TBL] [Abstract][Full Text] [Related]  

  • 6. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
    Zollino M; Murdolo M; Marangi G; Pecile V; Galasso C; Mazzanti L; Neri G
    Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):257-69. PubMed ID: 18932124
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 16p12.1 Deletion Orthologs are Expressed in Motile Neural Crest Cells and are Important for Regulating Craniofacial Development in
    Lasser M; Bolduc J; Murphy L; O'Brien C; Lee S; Girirajan S; Lowery LA
    Front Genet; 2022; 13():833083. PubMed ID: 35401697
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs.
    Altherr MR; Wright TJ; Denison K; Perez-Castro AV; Johnson VP
    Am J Med Genet; 1997 Jul; 71(1):47-53. PubMed ID: 9215768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Wolf-Hirschhorn syndrome: a case with normal karyotype, demonstrated by array CGH (aCGH).
    Saberi A; Shariati G; Hamid M; Galehdari H; Abdorasouli N
    Arch Iran Med; 2014 Sep; 17(9):642-4. PubMed ID: 25204484
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region.
    Wright TJ; Ricke DO; Denison K; Abmayr S; Cotter PD; Hirschhorn K; Keinänen M; McDonald-McGinn D; Somer M; Spinner N; Yang-Feng T; Zackai E; Altherr MR
    Hum Mol Genet; 1997 Feb; 6(2):317-24. PubMed ID: 9063753
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant to Young Teenager.
    Popescu DE; Marian D; Zeleniuc M; Samoila C; Belengeanu V
    Balkan J Med Genet; 2023 Jul; 26(1):75-82. PubMed ID: 37576793
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.
    Zollino M; Lecce R; Fischetto R; Murdolo M; Faravelli F; Selicorni A; Buttè C; Memo L; Capovilla G; Neri G
    Am J Hum Genet; 2003 Mar; 72(3):590-7. PubMed ID: 12563561
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization.
    Yang WX; Pan H; Li L; Wu HR; Wang ST; Bao XH; Jiang YW; Qi Y
    Chin Med J (Engl); 2016 Mar; 129(6):672-8. PubMed ID: 26960370
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
    Casaccia G; Mobili L; Braguglia A; Santoro F; Bagolan P
    Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mouse models for the Wolf-Hirschhorn deletion syndrome.
    Näf D; Wilson LA; Bergstrom RA; Smith RS; Goodwin NC; Verkerk A; van Ommen GJ; Ackerman SL; Frankel WN; Schimenti JC
    Hum Mol Genet; 2001 Jan; 10(2):91-8. PubMed ID: 11152656
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.
    Battaglia A; Filippi T; Carey JC
    Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):246-51. PubMed ID: 18932224
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distinct Epileptogenic Mechanisms Associated with Seizures in Wolf-Hirschhorn Syndrome.
    Corrêa T; Mayndra M; Santos-Rebouças CB
    Mol Neurobiol; 2022 May; 59(5):3159-3169. PubMed ID: 35278209
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical features in adult patient with Wolf-Hirschhorn syndrome.
    Martínez-Quintana E; Rodríguez-González F
    Morphologie; 2014 Jun; 98(321):86-9. PubMed ID: 24656633
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The Wolf-Hirschhorn Syndrome].
    Friebe-Hoffmann U; Reister F; Gaspar H; Hummler H; Lindner W; Lato K
    Z Geburtshilfe Neonatol; 2016 Oct; 220(5):195-199. PubMed ID: 27203859
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm.
    Callaway DA; Campbell IM; Stover SR; Hernandez-Garcia A; Jhangiani SN; Punetha J; Paine IS; Posey JE; Muzny D; Lally KP; Lupski JR; Shaw CA; Fernandes CJ; Scott DA
    J Pediatr Genet; 2018 Dec; 7(4):164-173. PubMed ID: 30430034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.