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 *

91 related articles for article (PubMed ID: 3499845)

  • 21. A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter).
    Lukusa T; Devriendt K; Fryns JP
    Ann Genet; 1999; 42(2):91-4. PubMed ID: 10434122
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Brief clinical report: duplication of distal 17q: report of an observation.
    Naccache NF; Vianna-Morgante AM; Richieri-Costa A
    Am J Med Genet; 1984 Mar; 17(3):633-9. PubMed ID: 6711615
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency.
    Pallotta R; Dalprà L; Miozzo M; Ehresmann T; Fusilli P
    Am J Med Genet; 2001 Dec; 104(4):282-6. PubMed ID: 11754060
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Autopsy findings in a severely affected infant with a 2q terminal deletion.
    Waters BL; Allen EF; Gibson PC; Johnston T
    Am J Med Genet; 1993 Nov; 47(7):1099-103. PubMed ID: 8291531
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
    Yu CW; Chen H; Baucum RW; Hand AM
    Ann Genet; 1981; 24(3):158-61. PubMed ID: 6974525
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
    Wang TH; Johnston K; Hsieh CL; Dennery PA
    Am J Med Genet; 1994 Feb; 49(4):399-401. PubMed ID: 8160733
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: a clinical and genetic study.
    Dubé P; Der Kaloustian VM ; Demczuk S; Saabti H; Koenekoop RK
    Ophthalmic Genet; 2000 Dec; 21(4):211-6. PubMed ID: 11135491
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocation.
    Chase TR; Jalal SM; Martsolf JT; Wasdahl WA
    Am J Med Genet; 1983 Feb; 14(2):347-51. PubMed ID: 6837629
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY.
    Scrideli CA; Baruffi MR; Squire JA; Ramos ES; Karaskova J; Heck B; Tone LG
    Leuk Res; 2005 Dec; 29(12):1465-7. PubMed ID: 15964069
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interstitial 1q43-q43 deletion with left ventricular noncompaction myocardium.
    Kanemoto N; Horigome H; Nakayama J; Ichida F; Xing Y; Buonadonna AL; Kanemoto K; Gentile M
    Eur J Med Genet; 2006; 49(3):247-53. PubMed ID: 16762826
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.
    Wenger SL; Boone LY; Cummins JH; Del Vecchio MA; Bay CA; Hummel M; Mowery-Rushton PA
    Am J Med Genet; 2000 Apr; 91(5):351-4. PubMed ID: 10766997
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Terminal 2q37 deletion and autistic behaviour.
    Lukusa T; Smeets E; Vogels A; Vermeesch JR; Fryns JP
    Genet Couns; 2005; 16(2):179-80. PubMed ID: 16080299
    [No Abstract]   [Full Text] [Related]  

  • 34. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL; Roberson J; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Jun; 46(4):438-40. PubMed ID: 7689299
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Partial 3q trisomy due to an unbalanced 3/10 translocation.
    Blumberg B; Moore R; Mohandas T
    Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Terminal deletion of (1)(q42) in a newborn.
    Montero MR; Martinez A; Fayos JL; Alvarez V
    Ann Genet; 1984; 27(3):178-9. PubMed ID: 6334483
    [No Abstract]   [Full Text] [Related]  

  • 37. Monosomy 1p36 deletion syndrome.
    Gajecka M; Mackay KL; Shaffer LG
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):346-56. PubMed ID: 17918734
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Two new cases of pure 1q terminal deletion presenting with brain malformations.
    Hiraki Y; Okamoto N; Ida T; Nakata Y; Kamada M; Kanemura Y; Yamasaki M; Fujita H; Nishimura G; Kato M; Harada N; Matsumoto N
    Am J Med Genet A; 2008 May; 146A(10):1241-7. PubMed ID: 18384145
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Terminal 6q25.3 deletion and abnormal behaviour.
    Lukusa T; Willekens D; Lukusa N; De Cock F; Fryns JP
    Genet Couns; 2001; 12(3):213-21. PubMed ID: 11693783
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.