BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 22365273)

  • 21. Introduction: advances in research on velo-cardio-facial syndrome/22q11.2 deletion syndrome.
    Kates WR; Emanuel BS
    Dev Disabil Res Rev; 2008; 14(1):1-2. PubMed ID: 18636630
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB; Chen E; Golabi M; Lebo RV
    Am J Med Genet; 1996 Dec; 66(3):250-6. PubMed ID: 8985481
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Deletion 22q11: spectrum of associated disorders.
    Hay BN
    Semin Pediatr Neurol; 2007 Sep; 14(3):136-9. PubMed ID: 17980310
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH
    Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
    Sullivan KE
    Immunol Allergy Clin North Am; 2008 May; 28(2):353-66. PubMed ID: 18424337
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 22q11 deletion syndrome: is that what they used to call . . . ?
    Umlauf MG
    Perspect Psychiatr Care; 2008 Oct; 44(4):259-66. PubMed ID: 18826464
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fragile X syndrome and 22q11.2 microdeletion in the same sibship.
    Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N
    Am J Med Genet; 2000 Dec; 95(4):358-60. PubMed ID: 11186890
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome].
    Pânzaru M; Rusu C; Voloşciuc M; Braha E; Butnariu L; Ivanov I; Grămescu M; Popescu R; Caba L; Sireteanu A; Macovei M; Covic M; Gorduza EV
    Rev Med Chir Soc Med Nat Iasi; 2011; 115(3):756-61. PubMed ID: 22046783
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.
    Shuib S; Abdul Latif Z; Abidin NZ; Akmal SN; Zakaria Z
    Malays J Pathol; 2009 Dec; 31(2):133-6. PubMed ID: 20514857
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. [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]  

  • 33. Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements.
    Emanuel BS
    Dev Disabil Res Rev; 2008; 14(1):11-8. PubMed ID: 18636632
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. The 22q11.2 deletion syndrome: more answers but more questions.
    Fernhoff PM
    J Pediatr; 2000 Aug; 137(2):145-7. PubMed ID: 10931401
    [No Abstract]   [Full Text] [Related]  

  • 36. [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]  

  • 37. Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.
    Edelmann L; Pandita RK; Morrow BE
    Am J Hum Genet; 1999 Apr; 64(4):1076-86. PubMed ID: 10090893
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Epilepsy in an adult with chromosome 22q11 micro-deletion].
    Alla P; Philip N; Azulay JP; Attarian S; Pouget J
    Rev Neurol (Paris); 1999 Nov; 155(11):967-70. PubMed ID: 10603642
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome.
    Babcock M; Yatsenko S; Hopkins J; Brenton M; Cao Q; de Jong P; Stankiewicz P; Lupski JR; Sikela JM; Morrow BE
    Hum Mol Genet; 2007 Nov; 16(21):2560-71. PubMed ID: 17675367
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.
    Unolt M; DiCairano L; Schlechtweg K; Barry J; Howell L; Kasperski S; Nance M; Adzick NS; Zackai EH; McDonald-McGinn DM
    Am J Med Genet A; 2017 Jan; 173(1):135-142. PubMed ID: 27682988
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.