BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 27197926)

  • 1. Severe laryngeal stenosis in newly born twins with 22q11.2 deletion syndrome: A case report.
    Clive B; Corsten G; Penney LS; Van den Hof M; El-Naggar W
    J Neonatal Perinatal Med; 2016 May; 9(2):223-6. PubMed ID: 27197926
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Laryngeal abnormalities are frequent in the 22q11 deletion syndrome.
    Leopold C; De Barros A; Cellier C; Drouin-Garraud V; Dehesdin D; Marie JP
    Int J Pediatr Otorhinolaryngol; 2012 Jan; 76(1):36-40. PubMed ID: 22019154
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Role of hypocalcemia in identification of 22q11 deletion syndrome among patients with congenital heart defects.
    de Mattos VF; Sulczinski LP; Milner OG; da Silva FA; de Moraes SA; Trevisan P; Fiegenbaum M; Varella-Garcia M; Zen PR; Rosa RF
    Int J Cardiol; 2014 Nov; 177(1):6-7. PubMed ID: 25499322
    [No Abstract]   [Full Text] [Related]  

  • 4. A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
    Vaz SO; Pires R; Pires LM; Carreira IM; Anjos R; Maciel P; Mota-Vieira L
    BMC Pediatr; 2015 Aug; 15():95. PubMed ID: 26297018
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [22Q11 microdeletion syndrome: cardiorespiratory symptoms and fibrobronchoscopy].
    Azpilicueta Idarreta M; Torres-Borrego J; Gilbert Pérez JJ; Ulloa Santamaría E; Frías Pérez M
    An Pediatr (Barc); 2012 Aug; 77(2):130-5. PubMed ID: 22459608
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Efficiency and good tolerance of rituximab for idiopathic thrombocytopenic purpura revealing a 22q11 deletion syndrome].
    Vautier M; Georgin-Lavialle S; Hermine O; Bienvenu B; Lacaze E; Gerard M; Aouba A
    Rev Med Interne; 2016 Nov; 37(11):766-770. PubMed ID: 26869291
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
    Bretelle F; Beyer L; Pellissier MC; Missirian C; Sigaudy S; Gamerre M; D'Ercole C; Philip N
    Eur J Med Genet; 2010; 53(6):367-70. PubMed ID: 20659598
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Catch-22? Wide variety of phenotypes associated with the chromosome 22q11 deletion syndrome in two patients].
    Till Á; Hadzsiev K; Lőcsei-Fekete A; Czakó M; Duga B; Melegh B
    Orv Hetil; 2015 Nov; 156(45):1834-8. PubMed ID: 26522857
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
    Yamagishi H; Ishii C; Maeda J; Kojima Y; Matsuoka R; Kimura M; Takao A; Momma K; Matsuo N
    Am J Med Genet; 1998 Jul; 78(4):319-21. PubMed ID: 9714432
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of anterior glottic webs with velocardiofacial syndrome (chromosome 22q11.2 deletion).
    Miyamoto RC; Cotton RT; Rope AF; Hopkin RJ; Cohen AP; Shott SR; Rutter MJ
    Otolaryngol Head Neck Surg; 2004 Apr; 130(4):415-7. PubMed ID: 15100636
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Newborn screening programs: should 22q11 deletion syndrome be added?
    Bales AM; Zaleski CA; McPherson EW
    Genet Med; 2010 Mar; 12(3):135-44. PubMed ID: 20071995
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Airway Anomalies in Patients With 22q11.2 Deletion Syndrome: A 5-Year Review.
    Jones JW; Tracy M; Perryman M; Arganbright JM
    Ann Otol Rhinol Laryngol; 2018 Jun; 127(6):384-389. PubMed ID: 29732908
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes.
    Vincent MC; Heitz F; Tricoire J; Bourrouillou G; Kuhlein E; Rolland M; Calvas P
    Genet Couns; 1999; 10(1):43-9. PubMed ID: 10191428
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Heart defects and other features of the 22q11 distal deletion syndrome.
    Fagerberg CR; Graakjaer J; Heinl UD; Ousager LB; Dreyer I; Kirchhoff M; Rasmussen AA; Lautrup CK; Birkebaek N; Sorensen K
    Eur J Med Genet; 2013 Feb; 56(2):98-107. PubMed ID: 23063575
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients.
    Fokstuen S; Bottani A; Medeiros PF; Antonarakis SE; Stoll C; Schinzel A
    Am J Med Genet; 1997 May; 70(2):130-3. PubMed ID: 9128930
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Laryngeal web with 22q11.2 deletion syndrome.
    Abe Y; Hirade T; Koike D; Matama C; Kato F
    Int J Pediatr Adolesc Med; 2022 Sep; 9(3):182-184. PubMed ID: 36090132
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of 22q11.2 deletion syndrome in twin pregnancy: a case report.
    Gul A; Gungorduk K; Turan I; Yildirim G; Gedikbasi A; Ozdemir A
    J Clin Ultrasound; 2013; 41 Suppl 1():6-9. PubMed ID: 22997003
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital cytomegalovirus infection among twin pairs.
    Egaña-Ugrinovic G; Goncé A; García L; Marcos MA; López M; Nadal A; Figueras F
    J Matern Fetal Neonatal Med; 2016 Nov; 29(21):3439-44. PubMed ID: 26689083
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment.
    Dufournet B; Nguyen K; Charles P; Grabli D; Jacquette A; Borg M; Danaila T; Mutez E; Drapier S; Colin O; Eusebio A; Philip N; Azulay JP
    Rev Neurol (Paris); 2017 Jun; 173(6):406-410. PubMed ID: 28461026
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Optimal Management of a 2-Hour-Old Newborn With Severe Congenital Subglottic Stenosis and Multiple Congenital Heart Diseases.
    Alshammari J; Alanazy S
    Ann Otol Rhinol Laryngol; 2015 Dec; 124(12):1006-10. PubMed ID: 26195575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.