BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 15930905)

  • 1. Tetrasomy 9q in an infant with cleft palate and multiple anomalies.
    McPherson E; Neiswanger K; Surti U
    Clin Dysmorphol; 2005 Jul; 14(3):145-147. PubMed ID: 15930905
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.
    El Khattabi L; Jaillard S; Andrieux J; Pasquier L; Perrin L; Capri Y; Benmansour A; Toutain A; Marcorelles P; Vincent-Delorme C; Journel H; Henry C; De Barace C; Devisme L; Dubourg C; Demurger F; Lucas J; Belaud-Rotureau MA; Amiel J; Malan V; De Blois MC; De Pontual L; Lebbar A; Le Dû N; Germain DP; Pinard JM; Pipiras E; Tabet AC; Aboura A; Verloes A
    Am J Med Genet A; 2015 Jun; 167(6):1252-61. PubMed ID: 25847481
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tetrasomy 9p: an emerging syndrome.
    Jalal SM; Kukolich MK; Garcia M; Benjamin TR; Day DW
    Clin Genet; 1991 Jan; 39(1):60-4. PubMed ID: 1997218
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
    Martín-De Saro MD; Valdés-Miranda JM; Plaza-Benhumea L; Pérez-Cabrera A; Gonzalez-Huerta LM; Guevara-Yañez R; Cuevas-Covarrubias SA
    Cytogenet Genome Res; 2015; 147(2-3):124-9. PubMed ID: 26900692
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three patients with terminal deletions within the subtelomeric region of chromosome 9q.
    Neas KR; Smith JM; Chia N; Huseyin S; St Heaps L; Peters G; Sholler G; Tzioumi D; Sillence DO; Mowat D
    Am J Med Genet A; 2005 Feb; 132A(4):425-30. PubMed ID: 15633179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22.
    Verheij JB; Bouman K; van Lingen RA; van Lookeren Campagne JG; Leegte B; van der Veen AY; Hofstra RM; Buys CH; van Essen AJ
    Am J Med Genet; 1999 Sep; 86(2):168-73. PubMed ID: 10449655
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.
    von Beust G; Sauter SM; Liehr T; Burfeind P; Bartels I; Starke H; von Eggeling F; Zoll B
    Am J Med Genet A; 2005 Aug; 137(1):59-64. PubMed ID: 16007665
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Duplication of 9q12-q33: a case report and implications for the dup(9q) syndrome.
    Stalker HJ; Aymé S; Delneste D; Scarpelli H; Vekemans M; Der Kaloustian VM
    Am J Med Genet; 1993 Feb; 45(4):456-9. PubMed ID: 8465850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
    Orye E; Verhaaren H; Van Egmond H; Devloo-Blancquaert A
    Clin Genet; 1975 Feb; 7(2):134-43. PubMed ID: 1132161
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG; Zackowski JL; Storto PD; Newlin A
    Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD; Hansen KL; Littlefield CA
    Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report.
    Pinto IP; Minasi LB; Steckelberg R; da Silva CC; da Cruz AD
    BMC Pediatr; 2018 Sep; 18(1):298. PubMed ID: 30193577
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Three cases of tetrasomy 9p.
    Dhandha S; Hogge WA; Surti U; McPherson E
    Am J Med Genet; 2002 Dec; 113(4):375-80. PubMed ID: 12457411
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Moving towards a syndrome: a review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survival.
    Tonk VS
    Clin Genet; 1997 Jul; 52(1):23-9. PubMed ID: 9272709
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report.
    Bellil H; Herve B; Herzog E; Ayoubi JM; Vialard F; Poulain M
    J Assist Reprod Genet; 2020 Mar; 37(3):573-577. PubMed ID: 31981038
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new case of 2q duplication supports either a locus for orofacial clefting between markers D2S1897 and D2S2023 or a locus for cleft palate only on chromosome 2q13-q21.
    Ounap K; Ilus T; Laidre P; Uibo O; Tammur P; Bartsch O
    Am J Med Genet A; 2005 Sep; 137A(3):323-7. PubMed ID: 16094674
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: case report and review of triplications and their possible mechanism.
    Wang J; Reddy KS; Wang E; Halderman L; Morgan BL; Lachman RS; Lin HJ; Cornford ME
    Am J Med Genet; 1999 Feb; 82(4):312-7. PubMed ID: 10051164
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.
    Gläser B; Rossier E; Barbi G; Chiaie LD; Blank C; Vogel W; Kehrer-Sawatzki H
    Am J Med Genet A; 2003 Jan; 116A(1):66-70. PubMed ID: 12476454
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome.
    Fryns JP
    Genet Couns; 1998; 9(3):229-30. PubMed ID: 9777347
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.