BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 7815448)

  • 21. CATCH22 syndrome with gastroesophageal reflux.
    Osaki Y; Oana S; Yasukawa K; Fujimori K; Terai M; Niimi H
    Pediatr Int; 2000 Aug; 42(4):367-8. PubMed ID: 10986867
    [No Abstract]   [Full Text] [Related]  

  • 22. Monozygotic twins with 22q11 deletion and discordant phenotypes.
    Fryer A
    J Med Genet; 1996 Feb; 33(2):173. PubMed ID: 8929959
    [No Abstract]   [Full Text] [Related]  

  • 23. CATCH 22.
    Hall JG
    J Med Genet; 1993 Oct; 30(10):801-2. PubMed ID: 8230153
    [No Abstract]   [Full Text] [Related]  

  • 24. [ Head and truncal abnormalities and secondary clinical aspects of 22q11 microdeletion. A series of 111 patients].
    Brevière GM; Croquette MF; Delobel B; Pellerin P; Rey C
    Arch Pediatr; 1999; 6 Suppl 2():305s-307s. PubMed ID: 10370516
    [No Abstract]   [Full Text] [Related]  

  • 25. Anomalous origin of the right pulmonary artery from the aorta and CATCH 22 syndrome.
    Johnson MC; Watson MS; Strauss AW; Spray TL
    Ann Thorac Surg; 1995 Sep; 60(3):681-2; discussion 682-3. PubMed ID: 7677500
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The search for hemizygosity at 22qll in patients with isolated cleft palate.
    Mingarelli R; Digilio MC; Mari A; Amati F; Standoli L; Giannotti A; Novelli G; Dallapiccola B
    J Craniofac Genet Dev Biol; 1996; 16(2):118-21. PubMed ID: 8773902
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.
    Driscoll DA; Spinner NB; Budarf ML; McDonald-McGinn DM; Zackai EH; Goldberg RB; Shprintzen RJ; Saal HM; Zonana J; Jones MC
    Am J Med Genet; 1992 Sep; 44(2):261-8. PubMed ID: 1360769
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Closing time for CATCH22.
    Burn J
    J Med Genet; 1999 Oct; 36(10):737-8. PubMed ID: 10528851
    [No Abstract]   [Full Text] [Related]  

  • 29. Increased nuchal translucency and CATCH 22.
    Lazanakis MS; Rodgers K; Economides DL
    Prenat Diagn; 1998 May; 18(5):507-10. PubMed ID: 9621387
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.
    McDonald-McGinn DM; LaRossa D; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Wang P; Solot C; Schultz P; Lynch D; Bingham P; Keenan G; Weinzimer S; Ming JE; Driscoll D; Clark BJ; Markowitz R; Cohen A; Moshang T; Pasquariello P; Randall P; Emanuel BS; Zackai EH
    Genet Test; 1997; 1(2):99-108. PubMed ID: 10464633
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome.
    Seaver LH; Pierpont JW; Erickson RP; Donnerstein RL; Cassidy SB
    J Med Genet; 1994 Nov; 31(11):830-4. PubMed ID: 7853364
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Presenting phenotype in 100 children with the 22q11 deletion syndrome.
    Oskarsdóttir S; Persson C; Eriksson BO; Fasth A
    Eur J Pediatr; 2005 Mar; 164(3):146-53. PubMed ID: 15565286
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Asymmetric crying facies associated with congenital hypoparathyroidism and 22q11 deletion.
    Akçakuş M; Güneş T; Kurtoğlu S; Cetin N; Ozkul Y; Narin N; Atabek ME; Uğraş R
    Turk J Pediatr; 2004; 46(2):191-3. PubMed ID: 15214756
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Is isolated palatal anomaly an indication to screen for 22q11 region deletion?
    Reish O; Finkelstein Y; Mesterman R; Nachmani A; Wolach B; Fejgin M; Amiel A
    Cleft Palate Craniofac J; 2003 Mar; 40(2):176-9. PubMed ID: 12605524
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Psychiatric inpatients and chromosome deletions within 22q11.2.
    Sugama S; Namihira T; Matsuoka R; Taira N; Eto Y; Maekawa K
    J Neurol Neurosurg Psychiatry; 1999 Dec; 67(6):803-6. PubMed ID: 10567504
    [TBL] [Abstract][Full Text] [Related]  

  • 37. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
    Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
    J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
    Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A
    Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects.
    Chaoui R; Kalache KD; Heling KS; Tennstedt C; Bommer C; Körner H
    Ultrasound Obstet Gynecol; 2002 Dec; 20(6):546-52. PubMed ID: 12493042
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region.
    Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J
    Eur J Pediatr Surg; 1993 Dec; 3 Suppl 1():27-8. PubMed ID: 8130147
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.