BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 28604963)

  • 1. [Phenotypic and genotypic analysis of a fetus carrying an intermediate 22q11.2 deletion encompassing the CRKL gene].
    Lin S; Zheng X; Gu H; Li M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):393-397. PubMed ID: 28604963
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Prenatal diagnosis of 22q11 microdeletion syndrome].
    Cai M; Huang H; Lin N; Guo N; Wu X; Su L; Xu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):192-195. PubMed ID: 28397216
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome.
    Lin I; Afshar Y; Goldstein J; Grossman J; Grody WW; Quintero-Rivera F
    Am J Med Genet A; 2021 Oct; 185(10):3042-3047. PubMed ID: 34196458
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genotype and phenotype study of two patients with 22q11.2 deletion syndrome].
    Zhu H; Wang A; Zhang H; Ji C; Zhan X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):623-7. PubMed ID: 25297596
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis by FISH of a 22q11 deletion in two families.
    Portnoï MF; Joyé N; Gonzales M; Demczuk S; Fermont L; Gaillard G; Bercau G; Morlier G; Taillemite JL
    J Med Genet; 1998 Feb; 35(2):165-8. PubMed ID: 9507401
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome.
    Koczkowska M; Wierzba J; Śmigiel R; Sąsiadek M; Cabała M; Ślężak R; Iliszko M; Kardaś I; Limon J; Lipska-Ziętkiewicz BS
    J Appl Genet; 2017 Feb; 58(1):93-98. PubMed ID: 27629806
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion.
    Oh DC; Min JY; Lee MH; Kim YM; Park SY; Won HS; Kim IK; Lee YH; Yoo SJ; Ryu HM
    J Korean Med Sci; 2002 Feb; 17(1):125-8. PubMed ID: 11850602
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome].
    Lin S; Luo Y; Wu J; Chen B; Ji Y; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):89-92. PubMed ID: 28186603
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
    Guris DL; Fantes J; Tara D; Druker BJ; Imamoto A
    Nat Genet; 2001 Mar; 27(3):293-8. PubMed ID: 11242111
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].
    Shi S; Pan G; Yang Y; Yan R; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):195-9. PubMed ID: 27060314
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genotype and phenotype analysis of a child with partial 18q deletion syndrome].
    Shi S; Guo L; Zha Q; Shi Z; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):567-570. PubMed ID: 28777861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotypic variability of atypical 22q11.2 deletions not including TBX1.
    Verhagen JM; Diderich KE; Oudesluijs G; Mancini GM; Eggink AJ; Verkleij-Hagoort AC; Groenenberg IA; Willems PJ; du Plessis FA; de Man SA; Srebniak MI; van Opstal D; Hulsman LO; van Zutven LJ; Wessels MW
    Am J Med Genet A; 2012 Oct; 158A(10):2412-20. PubMed ID: 22893440
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.
    Van Hemel JO; Schaap C; Van Opstal D; Mulder MP; Niermeijer MF; Meijers JH
    J Med Genet; 1995 Aug; 32(8):657-8. PubMed ID: 7473663
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.
    Shetty M; Srikanth A; Kadandale J; Hegde S
    Cytogenet Genome Res; 2016; 148(4):249-55. PubMed ID: 27300488
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genotype and phenotype studies on fetuses of 22q11.2 deletion syndrome].
    Zhu H; Zhang Y; Ji C; Li S; Niu Y; Zhang H; Chen L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):721-724. PubMed ID: 32619250
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Atypical deletion of 22q11.2: detection using the FISH TBX1 probe and molecular characterization with high-density SNP arrays.
    Beaujard MP; Chantot S; Dubois M; Keren B; Carpentier W; Mabboux P; Whalen S; Vodovar M; Siffroi JP; Portnoï MF
    Eur J Med Genet; 2009; 52(5):321-7. PubMed ID: 19467348
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of 22q11 in two brothers with different phenotype.
    Kasprzak L; Der Kaloustian VM; Elliott AM; Shevell M; Lejtenyi C; Eydoux P
    Am J Med Genet; 1998 Jan; 75(3):288-91. PubMed ID: 9475599
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2021 Jan; 60(1):165-168. PubMed ID: 33494995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.