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 *

214 related articles for article (PubMed ID: 29174092)

  • 1. Rare copy number variants identified in prune belly syndrome.
    Boghossian NS; Sicko RJ; Giannakou A; Dimopoulos A; Caggana M; Tsai MY; Yeung EH; Pankratz N; Cole BR; Romitti PA; Browne ML; Fan R; Liu A; Kay DM; Mills JL
    Eur J Med Genet; 2018 Mar; 61(3):145-151. PubMed ID: 29174092
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy number variations in a population with prune belly syndrome.
    Iqbal NS; Jascur TA; Harrison S; Chen C; Arevalo MK; Wong D; Sanchez E; Grimsby G; Wilson K; Baker LA
    Am J Med Genet A; 2018 Nov; 176(11):2276-2283. PubMed ID: 30285310
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare copy number variants implicated in posterior urethral valves.
    Boghossian NS; Sicko RJ; Kay DM; Rigler SL; Caggana M; Tsai MY; Yeung EH; Pankratz N; Cole BR; Druschel CM; Romitti PA; Browne ML; Fan R; Liu A; Brody LC; Mills JL
    Am J Med Genet A; 2016 Mar; 170(3):622-33. PubMed ID: 26663319
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare copy number variants in a population-based investigation of hypoplastic right heart syndrome.
    Dimopoulos A; Sicko RJ; Kay DM; Rigler SL; Druschel CM; Caggana M; Browne ML; Fan R; Romitti PA; Brody LC; Mills JL
    Birth Defects Res; 2017 Jan; 109(1):8-15. PubMed ID: 28009100
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case Report: Novel Copy Number Variant 16p11.2 Duplication Associated With Prune Belly Syndrome.
    Talluri S; Goedde MA; Rosenberg E; Canalichio KL; Peppas D; White JT
    Front Pediatr; 2021; 9():729932. PubMed ID: 34631626
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of prune belly syndrome.
    Xu W; Wu H; Wang DX; Mu ZH
    Pediatr Neonatol; 2015 Jun; 56(3):193-6. PubMed ID: 23639747
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prune Belly Syndrome in the Pig (Sus scrofa domesticus).
    Martín-Alguacil N; Avedillo L
    J Comp Pathol; 2020 Jan; 174():81-85. PubMed ID: 31955808
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dental treatment of patients with prune belly syndrome.
    Quilici G; Tolarova MM; Quilici M; Quilici DL
    Spec Care Dentist; 2023 Jan; 43(1):67-72. PubMed ID: 35526214
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene.
    Iqbal NS; Jascur TA; Harrison SM; Edwards AB; Smith LT; Choi ES; Arevalo MK; Chen C; Zhang S; Kern AJ; Scheuerle AE; Sanchez EJ; Xing C; Baker LA
    BMC Med Genet; 2020 Feb; 21(1):38. PubMed ID: 32085749
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of novel candidate disease genes from de novo exonic copy number variants.
    Gambin T; Yuan B; Bi W; Liu P; Rosenfeld JA; Coban-Akdemir Z; Pursley AN; Nagamani SCS; Marom R; Golla S; Dengle L; Petrie HG; Matalon R; Emrick L; Proud MB; Treadwell-Deering D; Chao HT; Koillinen H; Brown C; Urraca N; Mostafavi R; Bernes S; Roeder ER; Nugent KM; Bader PI; Bellus G; Cummings M; Northrup H; Ashfaq M; Westman R; Wildin R; Beck AE; Immken L; Elton L; Varghese S; Buchanan E; Faivre L; Lefebvre M; Schaaf CP; Walkiewicz M; Yang Y; Kang SL; Lalani SR; Bacino CA; Beaudet AL; Breman AM; Smith JL; Cheung SW; Lupski JR; Patel A; Shaw CA; Stankiewicz P
    Genome Med; 2017 Sep; 9(1):83. PubMed ID: 28934986
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prune-belly syndrome: ongoing controversies regarding pathogenesis and management.
    Wheatley JM; Stephens FD; Hutson JM
    Semin Pediatr Surg; 1996 May; 5(2):95-106. PubMed ID: 9138716
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copy number variants in hypoplastic right heart syndrome.
    Giannakou A; Sicko RJ; Kay DM; Zhang W; Romitti PA; Caggana M; Shaw GM; Jelliffe-Pawlowski LL; Mills JL
    Am J Med Genet A; 2018 Dec; 176(12):2760-2767. PubMed ID: 30289599
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion of hepatocyte nuclear factor-1-beta in an infant with prune belly syndrome.
    Haeri S; Devers PL; Kaiser-Rogers KA; Moylan VJ; Torchia BS; Horton AL; Wolfe HM; Aylsworth AS
    Am J Perinatol; 2010 Aug; 27(7):559-63. PubMed ID: 20175044
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number variants in Ebstein anomaly.
    Giannakou A; Sicko RJ; Zhang W; Romitti P; Browne ML; Caggana M; Brody LC; Jelliffe-Pawlowski L; Shaw GM; Kay DM; Mills JL
    PLoS One; 2017; 12(12):e0188168. PubMed ID: 29216221
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prune-Belly Syndrome: An Update.
    Conegundes AF; Garcia I; Miranda B; Borges A; Sanglard A; Ferreira G; Borges R; Simões E Silva AC
    Curr Pediatr Rev; 2024 Jun; ():. PubMed ID: 38879764
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prune-belly syndrome: case series and review of the literature regarding early prenatal diagnosis, epidemiology, genetic factors, treatment, and prognosis.
    Tonni G; Ida V; Alessandro V; Bonasoni MP
    Fetal Pediatr Pathol; 2013 Feb; 31(1):13-24. PubMed ID: 22506933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome.
    Amado NG; Nosyreva ED; Thompson D; Egeland TJ; Ogujiofor OW; Yang M; Fusco AN; Passoni N; Mathews J; Cantarel B; Baker LA; Syeda R
    Nat Commun; 2024 Jan; 15(1):339. PubMed ID: 38184690
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Contemporary epidemiology and characterization of newborn males with prune belly syndrome.
    Routh JC; Huang L; Retik AB; Nelson CP
    Urology; 2010 Jul; 76(1):44-8. PubMed ID: 20381841
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.
    Safizadeh Shabestari SA; Nassir N; Sopariwala S; Karimov I; Tambi R; Zehra B; Kosaji N; Akter H; Berdiev BK; Uddin M
    Hum Genet; 2023 Aug; 142(8):1201-1213. PubMed ID: 36383254
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copy number variations and cognitive phenotypes in unselected populations.
    Männik K; Mägi R; Macé A; Cole B; Guyatt AL; Shihab HA; Maillard AM; Alavere H; Kolk A; Reigo A; Mihailov E; Leitsalu L; Ferreira AM; Nõukas M; Teumer A; Salvi E; Cusi D; McGue M; Iacono WG; Gaunt TR; Beckmann JS; Jacquemont S; Kutalik Z; Pankratz N; Timpson N; Metspalu A; Reymond A
    JAMA; 2015 May; 313(20):2044-54. PubMed ID: 26010633
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.