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 *

207 related articles for article (PubMed ID: 4050847)

  • 1. Further delineation of the dup(3q) syndrome.
    Wilson GN; Dasouki M; Barr M
    Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
    Ayral D; Raudrant D; Charleux JP; Noel B
    Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP; Heck LJ; Carter GA; Flom JO
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3q.
    Rosenfeld W; Verma RS; Jhaveri RC; Estrada R; Evans H; Dosik H
    Am J Med Genet; 1981; 10(2):187-92. PubMed ID: 7315875
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly.
    Martin NJ; Steinberg BG
    Am J Med Genet; 1983 Apr; 14(4):767-72. PubMed ID: 6846406
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies.
    Mohammed FM; Farag TI; Gunawardana SS; al-Digashim DD; al-Awadi SA; al-Othman SA; Sundareshan TS
    Am J Med Genet; 1989 Mar; 32(3):353-5. PubMed ID: 2729356
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome.
    Ounap K; Ilus T; Bartsch O
    Am J Med Genet A; 2005 May; 134(4):434-8. PubMed ID: 15793836
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dup(1q)(q42-->qter) syndrome: case report and review of literature.
    Kennerknecht I; Barbi G; Rodens K
    Am J Med Genet; 1993 Dec; 47(8):1157-60. PubMed ID: 7507296
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
    Gonzalez CH; Billerbeck AE; Takayama LC; Wajntal A
    Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplication 3q syndrome: molecular delineation of the critical region.
    Aqua MS; Rizzu P; Lindsay EA; Shaffer LG; Zackai EH; Overhauser J; Baldini A
    Am J Med Genet; 1995 Jan; 55(1):33-7. PubMed ID: 7702094
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Duplication 3q(q21----qter) without limb anomalies.
    Ismail SR; Kousseff BG; Kotb SM; Kholeif SF
    Am J Med Genet; 1991 Mar; 38(4):518-22. PubMed ID: 2063889
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial duplication of distal 17q.
    Bridge J; Sanger W; Mosher G; Buehler B; Hearty C; Olney A; Fordyce R
    Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duplication of distal 15q: report of five new cases from two different translocation kindreds.
    Lacro RV; Jones KL; Mascarello JT; Jones OW; Wilson N; Jones MC
    Am J Med Genet; 1987 Mar; 26(3):719-28. PubMed ID: 3565485
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.
    Rizzu P; Haddad BR; Vallcorba I; Alonso A; Ferro MT; Garcia-Sagredo JM; Baldini A
    Am J Med Genet; 1997 Feb; 68(4):428-32. PubMed ID: 9021016
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome.
    Breslau EJ; Disteche C; Hall JG; Thuline H; Cooper P
    Am J Med Genet; 1981; 10(2):179-86. PubMed ID: 7315874
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation.
    Su PH; Chen JY; Chen SJ; Hung HM
    J Formos Med Assoc; 2004 Nov; 103(11):853-7. PubMed ID: 15549153
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.
    Bay C; Mauk J; Radcliffe J; Kaplan P
    Am J Med Genet; 1993 Nov; 47(7):965-8. PubMed ID: 7507294
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.