BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

319 related articles for article (PubMed ID: 16802747)

  • 1. [Neonatal hypocalcaemic dilated myocardiopathy due to a 22q11 microdeletion].
    Goulet M; Rio M; Jacquette A; Ladouceur M; Bonnet D
    Arch Mal Coeur Vaiss; 2006 May; 99(5):520-2. PubMed ID: 16802747
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypocalcemia and chromosome 22q11 microdeletion.
    Garabédian M
    Genet Couns; 1999; 10(4):389-94. PubMed ID: 10631928
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
    Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
    Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Transient neonatal hypocalcemia. Onset Manifestation of the 22q11.2 deletion syndrome].
    Pusceddu M; Bertone A; Campra D; Pontoriero D; Guala A
    Minerva Pediatr; 2002 Aug; 54(4):343-5. PubMed ID: 12131871
    [No Abstract]   [Full Text] [Related]  

  • 5. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G; Alvares S; Rocha C; Teixeira MF; Mota MC; Reis MI; Feijó MJ; Lima MR; Pinto MR
    Rev Port Cardiol; 2005 Mar; 24(3):349-71. PubMed ID: 15929620
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletion of chromosome 22q11 and pseudohypoparathyroidism.
    Craigen WJ; Lindsay EA; Bricker JT; Hawkins EP; Baldini A
    Am J Med Genet; 1997 Oct; 72(1):63-5. PubMed ID: 9295077
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
    Qin YF; Yang JB; Xie CH; Shao J; Zhao ZY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
    Carotti A; Digilio MC; Piacentini G; Saffirio C; Di Donato RM; Marino B
    Dev Disabil Res Rev; 2008; 14(1):35-42. PubMed ID: 18636635
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypocalcemia nutritional rickets: a curable cause of dilated cardiomyopathy.
    Verma S; Khadwal A; Chopra K; Rohit M; Singhi S
    J Trop Pediatr; 2011 Apr; 57(2):126-8. PubMed ID: 20554514
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
    Kitsiou-Tzeli S; Kolialexi A; Fryssira H; Galla-Voumvouraki A; Salavoura K; Kanariou M; Tsangaris GT; Kanavakis E; Mavrou A
    In Vivo; 2004; 18(5):603-8. PubMed ID: 15523900
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
    Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [DiGeorge syndrome, a review of 52 patients].
    Minier F; Carles D; Pelluard F; Alberti EM; Stern L; Saura R
    Arch Pediatr; 2005 Mar; 12(3):254-7. PubMed ID: 15734119
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A rare cause of reversible dilated cardiomyopathy: hypocalcemia.
    Avsar A; Dogan A; Tavli T
    Echocardiography; 2004 Oct; 21(7):609-12. PubMed ID: 15488088
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [CATCH22 or 22q11 deletion syndrome. An underdiagnosed and misunderstood disease category with a variable clinical picture].
    Oskarsdóttir S; Fasth A; Belfrage M; Viggedal G; Persson C; Eriksson BO
    Lakartidningen; 1999 Nov; 96(44):4789-93. PubMed ID: 10584540
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital cardiac defects with 22q11 deletion.
    Giray O; Ulgenalp A; Bora E; Sağin Saylam G; Unal N; Meşe T; Hüdaoğlu S; Erçal D
    Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Abdominal lymphatic dysplasia and 22q11 microdeletion.
    Mansir T; Lacombe D; Lamireau T; Taine L; Chateil JF; Le Bail B; Demarquez JL; Fayon M
    Genet Couns; 1999; 10(1):67-70. PubMed ID: 10191431
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic background of congenital conotruncal heart defects--a study of 45 families.
    Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
    Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.
    Iserin L; de Lonlay P; Viot G; Sidi D; Kachaner J; Munnich A; Lyonnet S; Vekemans M; Bonnet D
    Eur J Pediatr; 1998 Nov; 157(11):881-4. PubMed ID: 9835429
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Reversible hypokinetic cardiomyopathy revealing severe hypocalcemia].
    Charniot JC; Alexeeva A; Laurent S; Zerhouni K; Barthélemy B; Cohen R; Krivitzky A; Artigou JY
    Arch Mal Coeur Vaiss; 2001 Jul; 94(7):747-50. PubMed ID: 11494634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.