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 *

158 related articles for article (PubMed ID: 3117999)

  • 21. A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities.
    Elliott J; Maltby EL; Reynolds B
    J Med Genet; 1993 Mar; 30(3):251-2. PubMed ID: 7682620
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome.
    Engenheiro E; Saraiva J; Carreira I; Ramos L; Ropers HH; Silva E; Tommerup N; Tümer Z
    Clin Genet; 2007 Nov; 72(5):464-70. PubMed ID: 17850355
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review.
    Gambrelle J; Till M; Lukusa B; Beby F; Mory N; Sann L; Kodjikian L; Grange JD; Putet G
    Ophthalmic Genet; 2007 Jun; 28(2):105-9. PubMed ID: 17558854
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
    Zaletaev DV; Dadali EL; Kuleshov NP
    Tsitol Genet; 1987; 21(3):213-6. PubMed ID: 3617217
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4) (q25-->q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation.
    Schinzel A; Brecevic L; Dutly F; Baumer A; Binkert F; Largo RH
    J Med Genet; 1997 Dec; 34(12):1012-4. PubMed ID: 9429145
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension].
    Dressler P; Gramer E
    Ophthalmologe; 2006 May; 103(5):393-400. PubMed ID: 16683168
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
    Rauen KA; Albertson DG; Pinkel D; Cotter PD
    Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Different manifestation of Rieger syndrome in monozygotic twins.
    Geyer O; Loewenstein A; Garty BZ; Lazar M
    J Pediatr Ophthalmol Strabismus; 1994; 31(1):57-8. PubMed ID: 8195966
    [No Abstract]   [Full Text] [Related]  

  • 29. Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
    Wakazono A; Masuno M; Yamaguchi S; Tsubouchi K; Kondo N; Orii T
    Jpn J Hum Genet; 1992 Sep; 37(3):229-34. PubMed ID: 1472705
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Rieger syndrome].
    Ishikiriyama S
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):231-3. PubMed ID: 11057209
    [No Abstract]   [Full Text] [Related]  

  • 31. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG; Towner JW; Forsman I; Siris E
    Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
    Kamińska A; Sokołowska-Oracz A; Pawluczyk-Dyjecińska M; Szaflik JP
    Klin Oczna; 2007; 109(7-9):321-6. PubMed ID: 18260289
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Axenfeld-Rieger syndrome: report on dental and craniofacial findings.
    Jena AK; Kharbanda OP
    J Clin Pediatr Dent; 2005; 30(1):83-8. PubMed ID: 16302606
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24.
    Gladwin A; Donnai D; Metcalfe K; Schrander-Stumpel C; Brueton L; Verloes A; Aylsworth A; Toriello H; Winter R; Dixon M
    Hum Mol Genet; 1997 Jan; 6(1):123-7. PubMed ID: 9002680
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A new interstitial deletion of 4q (q21.1::q22.1).
    Fagan K; Gill A
    J Med Genet; 1989 Oct; 26(10):644-7. PubMed ID: 2585461
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tall stature and minor facial dysmorphisms in a patient with a 17.5 Mb interstitial deletion of chromosome 13 (q14.3q21.33): clinical report and review.
    van Bon BW; Koolen DA; Feenstra I; Neefs I; Pfundt R; Smeets DF; de Vries BB
    Clin Dysmorphol; 2007 Oct; 16(4):279-82. PubMed ID: 17786124
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features.
    Vande Perre P; Zazo Seco C; Patat O; Bouneau L; Vigouroux A; Bourgeois D; El Hout S; Chassaing N; Calvas P
    Eur J Med Genet; 2018 Feb; 61(2):72-78. PubMed ID: 29100920
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33.
    Tomkins DJ; Hunter AG; Uchida IA; Roberts MH
    Clin Genet; 1982 Dec; 22(6):348-55. PubMed ID: 7160106
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Interstitial deletion of chromosome 13: prognosis and adult phenotype.
    Dean JC; Simpson S; Couzin DA; Stephen GS
    J Med Genet; 1991 Aug; 28(8):533-5. PubMed ID: 1920369
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.