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 *

174 related articles for article (PubMed ID: 11339371)

  • 21. 22q11.2 Microduplication with thyroid hemiagenesis.
    Kim HJ; Jo HS; Yoo EG; Chung IH; Kim SW; Lee KH; Chang YH
    Horm Res Paediatr; 2013; 79(4):243-9. PubMed ID: 23364243
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Hypoparathyroidism and 22q11 deletion syndrome.
    Taylor SC; Morris G; Wilson D; Davies SJ; Gregory JW
    Arch Dis Child; 2003 Jun; 88(6):520-2. PubMed ID: 12765920
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Screening of patients at risk for 22q11 deletion.
    Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M
    Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.
    Kelly D; Goldberg R; Wilson D; Lindsay E; Carey A; Goodship J; Burn J; Cross I; Shprintzen RJ; Scambler PJ
    Am J Med Genet; 1993 Feb; 45(3):308-12. PubMed ID: 8434616
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Co-occurrence of 22q11 deletion syndrome and HDR syndrome.
    Fukai R; Ochi N; Murakami A; Nakashima M; Tsurusaki Y; Saitsu H; Matsumoto N; Miyake N
    Am J Med Genet A; 2013 Oct; 161A(10):2576-81. PubMed ID: 23918631
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome).
    Digilio MC; Giannotti A; Castro M; Colistro F; Ferretti F; Marino B; Dallapiccola B
    Am J Med Genet A; 2003 Sep; 121A(3):286-8. PubMed ID: 12923874
    [No Abstract]   [Full Text] [Related]  

  • 28. Bernard-Soulier syndrome associated with 22q11.2 deletion and clinical features of DiGeorge/velocardiofacial syndrome.
    Souto Filho JTD; Ribeiro HAA; Fassbender IPB; Ribeiro JMMC; Ferreira Júnior WDS; Figueiredo LCS
    Blood Coagul Fibrinolysis; 2019 Dec; 30(8):423-425. PubMed ID: 31738289
    [TBL] [Abstract][Full Text] [Related]  

  • 29. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.
    Bartsch O; Nemecková M; Kocárek E; Wagner A; Puchmajerová A; Poppe M; Ounap K; Goetz P
    Am J Med Genet A; 2003 Feb; 117A(1):1-5. PubMed ID: 12548732
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A patient with 22q11.2 deletion syndrome: case report.
    Eryılmaz SK; Baş F; Satan A; Darendeliler F; Bundak R; Günöz H; Saka N
    J Clin Res Pediatr Endocrinol; 2009; 1(3):151-4. PubMed ID: 21274400
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [The 22q11.2 deletion syndrome: immunological questions].
    Paśnik J; Cywińska-Bernas A; Piotrowicz M
    Postepy Hig Med Dosw (Online); 2007 Jun; 61():361-8. PubMed ID: 17572656
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A Rare Etiology of Hypocalcemic Seizures in Adulthood: Clues to Diagnosis from Facial Dysmorphism.
    Batra N; Kant R; Mandal K; Joshi K
    Neurol India; 2021; 69(1):161-163. PubMed ID: 33642291
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician.
    Thomas JA; Graham JM
    Clin Pediatr (Phila); 1997 May; 36(5):253-66. PubMed ID: 9152551
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions.
    Scirè G; Dallapiccola B; Iannetti P; Bonaiuto F; Galasso C; Mingarelli R; Boscherini B
    Am J Med Genet; 1994 Oct; 52(4):478-82. PubMed ID: 7747762
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Possible mechanisms and gene involvement in speech problems in the 22q11.2 deletion syndrome.
    Widdershoven JC; Beemer FA; Kon M; Dejonckere PH; Mink van der Molen AB
    J Plast Reconstr Aesthet Surg; 2008 Sep; 61(9):1016-23. PubMed ID: 18554997
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. CATCH 22 Syndrome.
    Yonehara Y; Nakatsuka T; Ichioka S; Sasaki N; Kobayashi T
    J Craniofac Surg; 2002 Sep; 13(5):623-6. PubMed ID: 12218787
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic basis of DiGeorge and velocardiofacial syndromes.
    Driscoll DA
    Curr Opin Pediatr; 1994 Dec; 6(6):702-6. PubMed ID: 7849818
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ocular findings in the chromosome 22q11.2 deletion syndrome.
    Forbes BJ; Binenbaum G; Edmond JC; DeLarato N; McDonald-McGinn DM; Zackai EH
    J AAPOS; 2007 Apr; 11(2):179-82. PubMed ID: 17140829
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.