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 *

183 related articles for article (PubMed ID: 22009409)

  • 1. Familial complex chromosomal rearrangement in a dysmorphic child with global developmental delay.
    Ngim CF; Keng WT; Ariffin R
    Singapore Med J; 2011 Oct; 52(10):e206-9. PubMed ID: 22009409
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
    Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
    Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G
    Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
    Curotti G; Benkhalifa M; Raybaud C; Picard F; Bellec V; Qumsiyeh MB
    Genet Couns; 1999; 10(3):259-64. PubMed ID: 10546097
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
    Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA; Pai GS; Stetten G
    Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
    Vundinti BR; Korgaonkar S; Ghosh K
    Gene; 2012 Apr; 498(1):128-30. PubMed ID: 22342255
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A unique combination of 17pter trisomy and 21qter monosomy in a boy with developmental delay, severe intellectual disability, growth retardation and dysmorphisms.
    Zheng Z; Yao RE; Geng J; Jin X; Shen Y; Ying D; Fu Q; Yu Y
    Gene; 2013 Mar; 516(2):301-6. PubMed ID: 23296059
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
    Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
    Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
    Guilherme RS; Cernach MC; Sfakianakis TE; Takeno SS; Nardozza LM; Rossi C; Bhatt SS; Liehr T; Melaragno MI
    Cytogenet Genome Res; 2013; 141(4):317-23. PubMed ID: 23817307
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
    Schürmann M; Wethling H; Niemeyer ML; Schwinger E
    Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
    [TBL] [Abstract][Full Text] [Related]  

  • 12. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
    Phelan MC; Blackburn W; Rogers RC; Crawford EC; Cooley NR; Schrock E; Ning Y; Ried T
    Prenat Diagn; 1998 Nov; 18(11):1174-80. PubMed ID: 9854728
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
    Repetto GM; Wagstaff J; Korf BR; Knoll JH
    Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.
    Popp S; Schulze B; Granzow M; Keller M; Holtgreve-Grez H; Schoell B; Brough M; Hager HD; Tariverdian G; Brown J; Kearney L; Jauch A
    Hum Genet; 2002 Jul; 111(1):31-9. PubMed ID: 12136233
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic analysis of a patient featuring developmental delay and mental retardation].
    Bai N; Liu Y; Mei S; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):208-11. PubMed ID: 27060317
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
    Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG; Spikes AS; Macha M; Dunn R
    J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
    Berend SA; Bodamer OA; Shapira SK; Shaffer LG; Bacino CA
    Am J Med Genet; 2002 May; 109(4):311-7. PubMed ID: 11992486
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.