These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 8481040)

  • 21. The DiGeorge anomaly (CATCH 22, DiGeorge/velocardiofacial syndrome).
    Hong R
    Semin Hematol; 1998 Oct; 35(4):282-90. PubMed ID: 9801257
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A case report of Noonan's syndrome with pulmonary valvar stenosis and coronary aneurysms.
    Loukas M; Dabrowski M; Kantoch M; Ruzyłło W; Waltenberger J; Giannikopoulos P
    Med Sci Monit; 2004 Dec; 10(12):CS80-3. PubMed ID: 15567989
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance.
    Pinto-Escalante D; Ceballos-Quintal JM; Castillo-Zapata I; Canto-Herrera J
    Am J Med Genet; 1998 Mar; 76(2):150-3. PubMed ID: 9511978
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial DiGeorge syndrome and associated partial monosomy of chromosome 22.
    Greenberg F; Crowder WE; Paschall V; Colon-Linares J; Lubianski B; Ledbetter DH
    Hum Genet; 1984; 65(4):317-9. PubMed ID: 6693120
    [TBL] [Abstract][Full Text] [Related]  

  • 25. An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.
    Lichtner P; König R; Hasegawa T; Van Esch H; Meitinger T; Schuffenhauer S
    J Med Genet; 2000 Jan; 37(1):33-7. PubMed ID: 10633131
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [The C heterochromatin of chromosomes 1, 9, 16 and Y in patients with Noonan's syndrome].
    Podugol'nikova OA; Solonichenko VG
    Tsitol Genet; 1994; 28(3):85-8. PubMed ID: 7974791
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Radiological features of late-onset lymphoedema in Noonan's syndrome.
    Ho WL; Wang JK; Li YW
    Pediatr Radiol; 2003 Mar; 33(3):200-2. PubMed ID: 12612821
    [TBL] [Abstract][Full Text] [Related]  

  • 28. DiGeorge syndrome and partial monosomy 10p: case report and review.
    Schuffenhauer S; Seidel H; Oechsler H; Belohradsky B; Bernsau U; Murken J; Meitinger T
    Ann Genet; 1995; 38(3):162-7. PubMed ID: 8540688
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2).
    Lupski JR; Langston C; Friedman R; Ledbetter DH; Greenberg F
    Am J Med Genet; 1991 Aug; 40(2):196-8. PubMed ID: 1897574
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Unusual combination of congenital heart lesions in a child with Noonan's syndrome.
    Lam J; Corno A; Oorthuys HW; Marcelletti C
    Pediatr Cardiol; 1982; 3(1):23-6. PubMed ID: 7155934
    [TBL] [Abstract][Full Text] [Related]  

  • 31. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
    Demczuk S; Aurias A
    Ann Genet; 1995; 38(2):59-76. PubMed ID: 7486827
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Turner's phenotype and diagnosis of Noonan's syndrome].
    Latini G; Berardi R
    Pediatr Med Chir; 1982; 4(5):535-8. PubMed ID: 6927352
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Large chondroma of the dural convexity in a patient with Noonan's syndrome. Case report and review of the literature.
    Delgado-López PD; Martín-Velasco V; Galacho-Harriero AM; Castilla-Díez JM; Rodríguez-Salazar A; Echevarría-Iturbe C
    Neurocirugia (Astur); 2007 Jun; 18(3):241-6. PubMed ID: 17622464
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [Cerebral defects in Noonan's syndrome (author's transl)].
    Görke W
    Klin Padiatr; 1980 Nov; 192(6):577-81. PubMed ID: 7194399
    [TBL] [Abstract][Full Text] [Related]  

  • 36. DiGeorge anomaly associated with 10p deletion.
    Monaco G; Pignata C; Rossi E; Mascellaro O; Cocozza S; Ciccimarra F
    Am J Med Genet; 1991 May; 39(2):215-6. PubMed ID: 2063928
    [TBL] [Abstract][Full Text] [Related]  

  • 37. In situ hybridization and translocation breakpoint mapping. III. DiGeorge syndrome with partial monosomy of chromosome 22.
    Cannizzaro LA; Emanuel BS
    Cytogenet Cell Genet; 1985; 39(3):179-83. PubMed ID: 3930157
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt.
    Čaplovičová M; Moslerová V; Dupej J; Macek M; Zemková D; Hoffmannová E; Havlovicová M; Velemínská J
    Am J Med Genet A; 2018 Dec; 176(12):2604-2613. PubMed ID: 30380201
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 22q11.2 syndrome due to maternal translocation t(18;22) (pl1.2;q11.2).
    Nur BG; Cetin Z; Clark OA; Mihci E; Oygur N; Karauzum SB
    Genet Couns; 2015; 26(1):67-75. PubMed ID: 26043510
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The deletions of 22q11--the Portuguese experience.
    Gaspar IM; Lourenço MT; Reis MI; Soares MA; Nogueira G; Ferreira F; Feijóo MJ
    Genet Couns; 1999; 10(1):51-7. PubMed ID: 10191429
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.