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 *

101 related articles for article (PubMed ID: 9629802)

  • 1. [Terminal 22q deletion: report of a case and review of the literature].
    Arroyo Carrera I; Barrio Sacristán AR; Romero Sala FJ; López Lafuente A; Villa Milla A
    An Esp Pediatr; 1998 Apr; 48(4):412-4. PubMed ID: 9629802
    [No Abstract]   [Full Text] [Related]  

  • 2. Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q).
    Herman GE; Greenberg F; Ledbetter DH
    Am J Med Genet; 1988 Apr; 29(4):909-15. PubMed ID: 3400736
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
    Taysi K; Strauss AW; Yang V; Padmalatha C; Marshall RE
    Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
    Chitayat D; Babul R; Silver MM; Jay V; Teshima IE; Babyn P; Becker LE
    Am J Med Genet; 1996 Jan; 61(1):45-8. PubMed ID: 8741917
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
    Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
    Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Terminal deletion of 6p: report of a new case.
    Plaja A; Vidal R; Soriano D; Bou X; Vendrell T; Mediano C; Pueyo JM; Labraña X; Sarret E
    Ann Genet; 1994; 37(4):196-9. PubMed ID: 7710255
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion.
    Phelan MC; Thomas GR; Saul RA; Rogers RC; Taylor HA; Wenger DA; McDermid HE
    Am J Med Genet; 1992 Jul; 43(5):872-6. PubMed ID: 1353666
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Terminal deletion of the long arm of chromosome 4:46,XY, del (4) (q31.3----qter: a case after in vitro fertilization].
    Lizarraga Azparren MA; Escudero Jiménez F; Lasarte Iradi JR; Sojo Aguirre A; Aramburu Bardesi N; Labayru Echebarría M; Tejada MI; Centeno Monterrubio C
    An Esp Pediatr; 1991 May; 34(5):404-6. PubMed ID: 1883118
    [No Abstract]   [Full Text] [Related]  

  • 10. Terminal deletion of chromosome 10q26 due to a paternal translocation [(7;10)(q36;q26)].
    Borovik CL; Brunoni D
    Am J Med Genet; 1991 Dec; 41(4):534-6. PubMed ID: 1776651
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. FISH-mapping of a 100-kb terminal 22q13 deletion.
    Anderlid BM; Schoumans J; Annerén G; Tapia-Paez I; Dumanski J; Blennow E; Nordenskjöld M
    Hum Genet; 2002 May; 110(5):439-43. PubMed ID: 12073014
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Deletion (13)(q22) with multiple congenital anomalies, hydranencephaly and penoscrotal transposition.
    Gershoni-Baruch R; Zekaria D
    Clin Dysmorphol; 1996 Oct; 5(4):289-94. PubMed ID: 8905192
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH.
    Smith A; St Heaps L; Robson L
    Am J Med Genet; 2002 Dec; 113(4):346-50. PubMed ID: 12457406
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qter.
    Talvik I; Ounap K; Bartsch O; Ilus T; Uibo O; Talvik T
    Am J Med Genet; 2000 Aug; 93(5):399-402. PubMed ID: 10951464
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial deletion of 22q11.2.
    Rodríguez Criado G; Gruesomontero J; Delicado Navarro A
    Genet Couns; 1999; 10(3):325-7. PubMed ID: 10546107
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.