BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 8456828)

  • 1. Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation.
    Shaffer LG; Hecht JT; Ledbetter DH; Greenberg F
    Am J Med Genet; 1993 Mar; 45(5):581-3. PubMed ID: 8456828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome.
    Wakui K; Gregato G; Ballif BC; Glotzbach CD; Bailey KA; Kuo PL; Sue WC; Sheffield LJ; Irons M; Gomez EG; Hecht JT; Potocki L; Shaffer LG
    Eur J Hum Genet; 2005 May; 13(5):528-40. PubMed ID: 15852040
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
    Wheeler PG; Weaver DD; Palmer CG
    Am J Med Genet; 1995 Feb; 55(4):462-5. PubMed ID: 7762587
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interstitial deletion of 11(p11.2p12): a newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2).
    Potocki L; Shaffer LG
    Am J Med Genet; 1996 Mar; 62(3):319-25. PubMed ID: 8882796
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial deletion of chromosome 18 (p11.2).
    Velagaleti GV; Harris S; Carpenter NJ; Coldwell J; Say B
    Ann Genet; 1996; 39(4):201-4. PubMed ID: 9037347
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mental retardation/shortness of stature/multiple minor anomalies syndrome associated with insertion of 3q material into 18p.
    al-Attia HM; Sedaghatian MR
    Am J Med Genet; 1995 Mar; 56(1):35-8. PubMed ID: 7747783
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family.
    de Pina Neto JM; Ferrari I
    Am J Med Genet; 1980; 5(1):25-33. PubMed ID: 7395898
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Duplication and deletion of chromosome band 2(p21p22) resulting from a familial interstitial insertion (2;11)(p21;p15).
    Sawyer JR; Jones E; Hawks FF; Quirk JG; Cunniff C
    Am J Med Genet; 1994 Feb; 49(4):422-7. PubMed ID: 8160737
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.
    Keppen LD; Gollin SM; Edwards D; Sawyer J; Wilson W; Overhauser J
    Am J Med Genet; 1992 Oct; 44(3):356-60. PubMed ID: 1488985
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7p15 leads to 7p21.
    Miller M; Kaufman G; Reed G; Bilenker R; Schinzel A
    Am J Med Genet; 1979; 4(4):323-32. PubMed ID: 539602
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Stratton RF; Dobyns WB; Greenberg F; DeSana JB; Moore C; Fidone G; Runge GH; Feldman P; Sekhon GS; Pauli RM
    Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion of 2p: a cytogenetic and clinical update.
    Neidich J; Zackai E; Aronson M; Emanuel BS
    Am J Med Genet; 1987 Jul; 27(3):707-10. PubMed ID: 3477100
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two families.
    Liberfarb RM; Breg WR; Atkins L; Holmes LB
    Am J Med Genet; 1979; 4(1):27-37. PubMed ID: 495650
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1).
    Berry R; Wilson H; Robinson J; Sandlin C; Tyson W; Campbell J; Porreco R; Manchester D
    Am J Med Genet; 1989 Nov; 34(3):358-65. PubMed ID: 2596525
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects.
    Wuyts W; Waeber G; Meinecke P; Schüler H; Goecke TO; Van Hul W; Bartsch O
    Eur J Hum Genet; 2004 May; 12(5):400-6. PubMed ID: 14872200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Supernumerary derivative (22) syndrome resulting from a maternal balanced translocation.
    Afroze B; Ngu LH; Roziana A; Aminah M; Noor Shahizan A
    Singapore Med J; 2008 Dec; 49(12):e372-4. PubMed ID: 19122939
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)].
    Freeman SB; Muralidharan K; Pettay D; Blackston RD; May KM
    Am J Med Genet; 1996 Feb; 61(4):340-4. PubMed ID: 8834045
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and molecular analyses of deletion 3p25-pter syndrome.
    Mowrey PN; Chorney MJ; Venditti CP; Latif F; Modi WS; Lerman MI; Zbar B; Robins DB; Rogan PK; Ladda RL
    Am J Med Genet; 1993 Jul; 46(6):623-9. PubMed ID: 8103286
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
    Blennow E; Bui TH; Wallin A; Kogner P
    Am J Med Genet; 1996 Oct; 65(1):60-7. PubMed ID: 8914743
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
    Martínez-Garay I; Tomás M; Oltra S; Ramser J; Moltó MD; Prieto F; Meindl A; Kutsche K; Martínez F
    Eur J Hum Genet; 2007 Jan; 15(1):29-34. PubMed ID: 17033686
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.