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 *

97 related articles for article (PubMed ID: 7815441)

  • 1. Familial half cryptic translocation t(9;17).
    Köhler A; Hain J; Müller U
    J Med Genet; 1994 Sep; 31(9):712-4. PubMed ID: 7815441
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Miller-Dieker syndrome. Detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring.
    Alvarado M; Bass HN; Caldwell S; Jamehdor M; Miller AA; Jacob P
    Am J Dis Child; 1993 Dec; 147(12):1291-4. PubMed ID: 8249946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
    Bacino CA; Kashork CD; Davino NA; Shaffer LG
    Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.
    Kuwano A; Ledbetter SA; Dobyns WB; Emanuel BS; Ledbetter DH
    Am J Hum Genet; 1991 Oct; 49(4):707-14. PubMed ID: 1897521
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cryptic translocation t(5;18) in familial mental retardation.
    Vogels A; Devriendt K; Vermeesch JR; Van Dael R; Marynen P; Dewaele P; Hageman J; Holvoet M; Fryns JP
    Ann Genet; 2000; 43(3-4):117-23. PubMed ID: 11164192
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).
    Liehr T; Heller A; Eichhorn KH; Beensen V; Schulze E; Starke H; Claussen U; Schreyer I
    Prenat Diagn; 2004 Dec; 24(12):1022-4. PubMed ID: 15614895
    [No Abstract]   [Full Text] [Related]  

  • 7. Miller-Dieker syndrome due to maternal cryptic translocation t(10;17) (q26.3;p13.3).
    Masuno M; Imaizumi K; Nakamura M; Matsui K; Goto A; Kuroki Y
    Am J Med Genet; 1995 Dec; 59(4):441-3. PubMed ID: 8585563
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).
    Holinski-Feder E; Reyniers E; Uhrig S; Golla A; Wauters J; Kroisel P; Bossuyt P; Rost I; Jedele K; Zierler H; Schwab S; Wildenauer D; Speicher MR; Willems PJ; Meitinger T; Kooy RF
    Am J Hum Genet; 2000 Jan; 66(1):16-25. PubMed ID: 10631133
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal and postnatal investigation of a case with Miller-Dieker syndrome due to a familial cryptic translocation t(17;20) (p13.3;q13.3) detected by fluorescence in situ hybridization.
    van Zelderen-Bhola SL; Breslau-Siderius EJ; Beverstock GC; Stolte-Dijkstra I; de Vries LS; Stoutenbeek P; de Pater JM
    Prenat Diagn; 1997 Feb; 17(2):173-9. PubMed ID: 9061768
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study.
    Reid E; Morrison N; Barron L; Boyd E; Cooke A; Fielding D; Tolmie JL
    J Med Genet; 1996 Mar; 33(3):197-202. PubMed ID: 8728691
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.
    Wieczorek D; Engels H; Viersbach R; Henke B; Schwanitz G; Passarge E
    J Med Genet; 1998 Jul; 35(7):545-53. PubMed ID: 9678698
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6.
    Groen SE; Drewes JG; de Boer EG; Hoovers JM; Hennekam RC
    Am J Med Genet; 1998 Dec; 80(5):448-53. PubMed ID: 9880207
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
    Senger G; Chudoba I; Friedrich U; Tommerup N; Claussen U; Brøndum-Nielsen K
    Prenat Diagn; 1997 Apr; 17(4):369-74. PubMed ID: 9160390
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Familial Miller-Dieker syndrome and (15;17) chromosome translocation].
    Goutières F; Aicardi J; Rethore MO; Prieur M; Lejeune J
    Arch Fr Pediatr; 1987; 44(7):501-4. PubMed ID: 3426372
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Six cases of deletion 9p24 and trisomy 19q13.4 inherited from a familial balanced translocation.
    Su PH; Kuo PL; Chen SJ; Huang SC; Chen JY; Hung HM
    J Formos Med Assoc; 2005 Jul; 104(7):525-30. PubMed ID: 16091833
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S; Aypar E; Beksaç MS; Bartsch O
    Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial mental retardation due to a cryptic subtelomeric translocation -del 14qter and dup 9qter (the Anyon phenotype).
    Lowry RB; Baker E; Dixon J; Hinton L
    Clin Dysmorphol; 2007 Oct; 16(4):223-9. PubMed ID: 17786113
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case report. Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome.
    Abreu LS; Brassesco MS; Moreira ML; Pina-Neto JM
    Genet Mol Res; 2014 Jun; 13(2):4302-10. PubMed ID: 25036174
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial translocation t(9;16).
    Dowman C; Lockwood D; Allanson J
    J Med Genet; 1989 Aug; 26(8):525-8. PubMed ID: 2671373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.