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 *

60 related articles for article (PubMed ID: 2801781)

  • 1. Apparently balanced chromosome translocations and midline defects.
    Cowchock S
    Am J Med Genet; 1989 Jul; 33(3):424. PubMed ID: 2801781
    [No Abstract]   [Full Text] [Related]  

  • 2. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
    Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F
    Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646
    [TBL] [Abstract][Full Text] [Related]  

  • 3. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21).
    de Almeida JC; Reis DF; Llerena JC; Pereira ET
    Ann Genet; 1989; 32(3):181-3. PubMed ID: 2817779
    [TBL] [Abstract][Full Text] [Related]  

  • 4. "Understanding Adam" multiple reciprocal translocations: complex case presentation.
    Linder CE; Lu X; Kim YM; Li S; Pineda J
    J Perinat Neonatal Nurs; 2009; 23(2):150-6; quiz 157-8. PubMed ID: 19474586
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lack of linkage of apparently dominant cleft lip (palate) to two candidate chromosomal regions.
    Pierpont JW; Storm AL; Erickson RP; Kohn BR; Pettijohn L; DePaepe A
    J Craniofac Genet Dev Biol; 1995; 15(2):66-71. PubMed ID: 7635931
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Split-foot anomaly, microphthalmia, cleft-lip and cleft-palate, and mental retardation associated with a chromosome 6;13 translocation.
    Viljoen DL; Smart R
    Clin Dysmorphol; 1993 Jul; 2(3):274-7. PubMed ID: 8287191
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 10p duplication characterized by fluorescence in situ hybridization.
    Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
    Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy].
    Tenconi R; Baccichetti C; Dussini N; Panizza G
    Ann Genet; 1974 Dec; 17(4):275-7. PubMed ID: 4281288
    [No Abstract]   [Full Text] [Related]  

  • 10. Constitutional balanced translocations in patients with solid tumors.
    Richard F; Muleris M; Couturier J; Gerbault-Seureau M; Lombard M; Dutrillaux B
    Cancer Genet Cytogenet; 1992 Jul; 61(1):50-2. PubMed ID: 1638480
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Peters anomaly in association with multiple midline anomalies and a familial chromosome 4 inversion.
    Neilan E; Pikman Y; Kimonis VE
    Ophthalmic Genet; 2006 Jun; 27(2):63-5. PubMed ID: 16754208
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital heart defect in a patient with deletion of chromosome 7q.
    Tiller GE; Watson MS; Duncan LM; Dowton SB
    Am J Med Genet; 1988 Feb; 29(2):283-7. PubMed ID: 3354600
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Promiscuous translocations of chromosome arm 17q in human neuroblastomas.
    Lastowska M; Roberts P; Pearson AD; Lewis I; Wolstenholme J; Bown N
    Genes Chromosomes Cancer; 1997 Jul; 19(3):143-9. PubMed ID: 9218994
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
    Zeiger JS; Hetmanski JB; Beaty TH; VanderKolk CA; Wyszynski DF; Bailey-Wilson JE; de Luna RO; Perandones C; Tolarova MM; Mosby T; Bennun R; Segovia M; Calda P; Pugh EW; Doheny K; McIntosh I
    Eur J Hum Genet; 2003 Nov; 11(11):835-9. PubMed ID: 14571267
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: a case report.
    Moradkhani K; Puechberty J; Bhatt S; Lespinasse J; Vago P; Lefort G; Sarda P; Hamamah S; Pellestor F
    Hum Reprod; 2006 Dec; 21(12):3193-8. PubMed ID: 16917122
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH.
    Delneste D; Vamos E; Pierquin G; Hayez-Delatte F; Van Regemorter N
    Genet Couns; 1998; 9(2):97-102. PubMed ID: 9664205
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
    Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome translocations in B and T cell neoplasias.
    Showe LC; Croce CM
    Semin Hematol; 1986 Oct; 23(4):237-44. PubMed ID: 3535082
    [No Abstract]   [Full Text] [Related]  

  • 20. Female gamete segregation in two carriers of translocations involving 2q and 14q.
    Escudero T; Lee M; Sandalinas M; Munné S
    Prenat Diagn; 2000 Mar; 20(3):235-7. PubMed ID: 10719328
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.