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 *

105 related articles for article (PubMed ID: 15372521)

  • 1. Partial tetrasomy 15 due to a unique inverted triplication of chromosome15q24-q26.
    James PA; Aftimos S; Oei P
    Am J Med Genet A; 2004 Oct; 130A(2):208-10. PubMed ID: 15372521
    [No Abstract]   [Full Text] [Related]  

  • 2. Intrachromosomal triplication for the distal part of chromosome 15q.
    Schluth C; Mattei MG; Mignon-Ravix C; Salman S; Alembik Y; Willig J; Ginglinger E; Jeandidier E
    Am J Med Genet A; 2005 Jul; 136(2):179-84. PubMed ID: 15940678
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A child with bisatellited, dicentric chromosome 15 arising from a maternal paracentric inversion of chromosome 15q.
    Whiteford ML; Baird C; Kinmond S; Donaldson B; Davidson HR
    J Med Genet; 2000 Aug; 37(8):E11. PubMed ID: 10922391
    [No Abstract]   [Full Text] [Related]  

  • 4. De novo duplication of the short arm of chromosome 12: dup(12)(p13.1p13.3).
    Tsai AC; Digiovanni M; Walton C; Cotter PD
    Am J Med Genet A; 2005 Apr; 134A(2):229-30. PubMed ID: 15633165
    [No Abstract]   [Full Text] [Related]  

  • 5. Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report.
    Nietzel A; Albrecht B; Starke H; Heller A; Gillessen-Kaesbach G; Claussen U; Liehr T
    J Med Genet; 2003 Mar; 40(3):e28. PubMed ID: 12624157
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. Intrachromosomal triplication 12p11.22-p12.3 and gonadal mosaicism of partial tetrasomy 12p.
    Eckel H; Wimmer R; Volleth M; Jakubiczka S; Muschke P; Wieacker P
    Am J Med Genet A; 2006 Jun; 140(11):1219-22. PubMed ID: 16652358
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13.
    Mehra S; Christ L; Jeng L; Zinn AB; Schwartz S
    Am J Med Genet A; 2005 Aug; 137(2):217-21. PubMed ID: 16059944
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of an unusual marker chromosome by spectral karyotyping.
    Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
    Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
    Abuelo D; Mark HF; Bier JA
    Clin Pediatr (Phila); 1995 Apr; 34(4):223-6. PubMed ID: 7540523
    [No Abstract]   [Full Text] [Related]  

  • 11. Unmasking 15q12 deletion using microarray-based comparative genomic hybridization in a mentally retarded boy with r(Y).
    Kurosawa K; Harada N; Sosonkina N; Niikawa N; Matsumoto N; Saitoh S
    Am J Med Genet A; 2004 Oct; 130A(3):322-4. PubMed ID: 15378544
    [No Abstract]   [Full Text] [Related]  

  • 12. Delineation of the cryptic 1qter deletion phenotype.
    Merritt JL; Zou Y; Jalal SM; Michels VV
    Am J Med Genet A; 2007 Mar; 143A(6):599-603. PubMed ID: 17304549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion 2p15-16.1 syndrome: case report and review.
    Prontera P; Bernardini L; Stangoni G; Capalbo A; Rogaia D; Romani R; Ardisia C; Dallapiccola B; Donti E
    Am J Med Genet A; 2011 Oct; 155A(10):2473-8. PubMed ID: 21910216
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial tetrasomy 11q resulting from an intrachromosomal triplication of a 22 Mb region of chromosome 11.
    Kekis M; Deeg C; Hashimoto S; McKinney A; Erdman L; Green-Geer C; Shuss C; Hickey S; Astbury C; Pyatt RE
    Am J Med Genet A; 2017 Apr; 173(4):1056-1060. PubMed ID: 28328127
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy of 15q due to inserted inverted duplication.
    Elçioglu N; Fear C; Berry AC
    Clin Genet; 1997 Dec; 52(6):442-5. PubMed ID: 9520256
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl.
    Barbi G; Spaich C; Adolph S; Kehrer-Sawatzki H
    J Med Genet; 2003 Mar; 40(3):e27. PubMed ID: 12624156
    [No Abstract]   [Full Text] [Related]  

  • 18. Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.
    Long FL; Duckett DP; Billam LJ; Williams DK; Crolla JA
    J Med Genet; 1998 May; 35(5):425-8. PubMed ID: 9610809
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.