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 *

196 related articles for article (PubMed ID: 28018437)

  • 1. 1p36 deletion syndrome confirmed by fluorescence
    Kang DS; Shin E; Yu J
    Korean J Pediatr; 2016 Nov; 59(Suppl 1):S14-S18. PubMed ID: 28018437
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
    D'Angelo CS; Da Paz JA; Kim CA; Bertola DR; Castro CI; Varela MC; Koiffmann CP
    Eur J Med Genet; 2006; 49(6):451-60. PubMed ID: 16564757
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
    Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA
    Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
    Hussen DF; Kamel AK; Mekkawy MK; Ashaat EA; El Ruby MO
    Mol Syndromol; 2020 Dec; 11(5-6):284-295. PubMed ID: 33510599
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.
    Seo GH; Kim JH; Cho JH; Kim GH; Seo EJ; Lee BH; Choi JH; Yoo HW
    Korean J Pediatr; 2016 Jan; 59(1):16-23. PubMed ID: 26893599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 1p36 deletion syndrome: first case report in Morocco detected by fluorescence
    Dafir K; Bouzid FZ; Mansouri M; Aboussair N
    Pan Afr Med J; 2020; 37():349. PubMed ID: 33738037
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Monosomy 1p36 deletion syndrome.
    Gajecka M; Mackay KL; Shaffer LG
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):346-56. PubMed ID: 17918734
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.
    Kurosawa K; Kawame H; Okamoto N; Ochiai Y; Akatsuka A; Kobayashi M; Shimohira M; Mizuno S; Wada K; Fukushima Y; Kawawaki H; Yamamoto T; Masuno M; Imaizumi K; Kuroki Y
    Brain Dev; 2005 Aug; 27(5):378-82. PubMed ID: 16023556
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
    Shimojima K; Páez MT; Kurosawa K; Yamamoto T
    Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis.
    Cho EK; Kim J; Yang A; Cho SY; Jin DK
    Ann Pediatr Endocrinol Metab; 2017 Jun; 22(2):129-132. PubMed ID: 28690993
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.
    Shapira SK; McCaskill C; Northrup H; Spikes AS; Elder FF; Sutton VR; Korenberg JR; Greenberg F; Shaffer LG
    Am J Hum Genet; 1997 Sep; 61(3):642-50. PubMed ID: 9326330
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review.
    Greco M; Ferrara P; Farello G; Striano P; Verrotti A
    Epilepsy Res; 2018 Jan; 139():92-101. PubMed ID: 29212048
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report.
    Fitzgibbon GJ; Clayton-Smith J; Banka S; Hamilton SJ; Needham MM; Dore JK; Miller JT; Pawson GD; Gaunt L
    J Med Case Rep; 2008 Nov; 2():355. PubMed ID: 19019217
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36.
    Lissauer D; Larkins SA; Sharif S; MacPherson L; Rhodes C; Kilby MD
    Prenat Diagn; 2007 Sep; 27(9):874-8. PubMed ID: 17582615
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [An updated review of 1p36 deletion (monosomy) syndrome].
    Bello S; Rodríguez-Moreno A
    Rev Chil Pediatr; 2016; 87(5):411-421. PubMed ID: 26875550
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Morbid obesity in a child with monosomy 1p36 syndrome.
    Zagalo A; Dias P; Pereira C; Sampaio Mde L
    BMJ Case Rep; 2012 Mar; 2012():. PubMed ID: 22605691
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.
    Isidor B; Le Cunff M; Boceno M; Boisseau P; Thomas C; Rival JM; David A; Le Caignec C
    Eur J Med Genet; 2008; 51(6):679-84. PubMed ID: 18672103
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.