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 *

133 related articles for article (PubMed ID: 1609823)

  • 1. Nonrandom association of atrioventricular canal and del (8p) syndrome.
    Marino B; Reale A; Giannotti A; Digilio MC; Dallapiccola B
    Am J Med Genet; 1992 Feb; 42(4):424-7. PubMed ID: 1609823
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.
    Nienhaus H; Mau U; Zang KD
    Am J Med Genet; 1992 Nov; 44(5):573-5. PubMed ID: 1481811
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
    Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiple congenital anomalies, thymic dysplasia, severe congenital heart disease, and oligosyndactyly with a deletion of the short arm of chromosome 5.
    Taylor MJ; Josifek K
    Am J Med Genet; 1981; 9(1):5-11. PubMed ID: 6264787
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML; Ryan RM
    Am J Med Genet; 1995 Mar; 56(1):97-100. PubMed ID: 7747796
    [TBL] [Abstract][Full Text] [Related]  

  • 6. GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease.
    Pehlivan T; Pober BR; Brueckner M; Garrett S; Slaugh R; Van Rheeden R; Wilson DB; Watson MS; Hing AV
    Am J Med Genet; 1999 Mar; 83(3):201-6. PubMed ID: 10096597
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.
    Wu BL; Schneider GH; Sabatino DE; Bozovic LZ; Cao B; Korf BR
    Am J Med Genet; 1996 Mar; 62(1):77-83. PubMed ID: 8779331
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
    Gibbons B; Tan SY; Kee SK; Quaife R; Lim ST
    Am J Med Genet; 1999 Sep; 86(3):289-93. PubMed ID: 10482883
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8p.
    Amati F; Mari A; Mingarelli R; Gennarelli M; Digilio MC; Giannotti A; Marino B; Novelli G; Dallapiccola B
    Am J Med Genet; 1995 Jul; 57(3):483-8. PubMed ID: 7677156
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion of terminal portion of 6q: report of a case with unusual malformations.
    Shen-Schwarz S; Hill LM; Surti U; Marchese S
    Am J Med Genet; 1989 Jan; 32(1):81-6. PubMed ID: 2705486
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Heart disease associated with deletion of the short arm of chromosome 18.
    Movahhedian HR; Kane HA; Borgaonkar D; McDermott M; Septimus S
    Del Med J; 1991 May; 63(5):285-9. PubMed ID: 1860515
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM; Sekhon GS; Laxova R
    Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions.
    Verheij JB; de Munnik SA; Dijkhuizen T; de Leeuw N; Olde Weghuis D; van den Hoek GJ; Rijlaarsdam RS; Thomasse YE; Dikkers FG; Marcelis CL; van Ravenswaaij-Arts CM
    Eur J Med Genet; 2009; 52(5):353-7. PubMed ID: 19464398
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
    Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interstitial deletion 2q31 leads to q33.
    Buchanan PD; Rhodes RL; Stevenson CE
    Am J Med Genet; 1983 May; 15(1):121-6. PubMed ID: 6683075
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.
    Fryns JP; Kleczkowska A; Van den Berghe H
    Ann Genet; 1990; 33(1):43-5. PubMed ID: 2195980
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.