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 *

115 related articles for article (PubMed ID: 9950373)

  • 61. Interstitial Dup(1p) with findings of Kabuki make-up syndrome.
    Lo IF; Cheung LY; Ng AY; Lam ST
    Am J Med Genet; 1998 Jun; 78(1):55-7. PubMed ID: 9637424
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Familial insertional translocation of a portion of 3q into 11q resulting in duplication and deletion of region 3q22.1 leads to q24 in different offspring.
    Williamson RA; Donlan MA; Dolan CR; Thuline HC; Harrison MT; Hall JG
    Am J Med Genet; 1981; 9(2):105-11. PubMed ID: 7258223
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers.
    Arens YH; Engelen JJ; Govaerts LC; van Ravenswaay CM; Loneus WH; van Lent-Albrechts JC; van der Blij-Philipsen M; Hamers AJ; Schrander-Stumpel CT
    Am J Med Genet A; 2004 Oct; 130A(2):128-33. PubMed ID: 15372532
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Follow-up of a familial translocation t(10;16) with an unusual segregation pattern.
    Resta RG; Luthardt F; Kapur R
    Am J Med Genet; 1996 May; 63(2):363-5. PubMed ID: 8725786
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Autosomal insertional translocation mimicking an X-linked mode of inheritance.
    Thierry G; Pichon O; Briand A; Poulain D; Sznajer Y; David A; Le Caignec C
    Eur J Med Genet; 2013 Jan; 56(1):46-9. PubMed ID: 23107885
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Interchromosomal insertions. Identification of five cases and a review.
    Van Hemel JO; Eussen HJ
    Hum Genet; 2000 Nov; 107(5):415-32. PubMed ID: 11140939
    [TBL] [Abstract][Full Text] [Related]  

  • 67. De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISH.
    Sanchez-Garcia JF; de Die-Smulders CE; Weber JW; Jetten AG; Loneus WH; Hamers AJ; Engelen JJ
    Am J Med Genet; 2001 Apr; 100(1):56-61. PubMed ID: 11337750
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Interstitial deletion 13q31 associated with normal phenotype: cytogenetic study of a family with concomitant segregation of reciprocal translocation and interstitial deletion.
    Ke YY; Lee DJ; Ma GC; Lee MH; Wang BT; Chen M
    J Formos Med Assoc; 2007 Jul; 106(7):582-8. PubMed ID: 17660149
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Recurring breakpoints of 1p13 approximately p22 in osteochondroma.
    Sawyer JR; Thomas EL; Lukacs JL; Swanson CM; Ding Y; Parham DM; Thomas JR; Nicholas RW
    Cancer Genet Cytogenet; 2002 Oct; 138(2):102-6. PubMed ID: 12505252
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Molecular and clinical characterization of a patient with duplication of 1p36.3 and metopic synostosis.
    Heilstedt HA; Shapira SK; Gregg AR; Shaffer LG
    Clin Genet; 1999 Aug; 56(2):123-8. PubMed ID: 10517248
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Syndromal obesity due to paternal duplication 6(q24.3-q27).
    Smith A; Jauch A; Slater H; Robson L; Sandanam T
    Am J Med Genet; 1999 May; 84(2):125-31. PubMed ID: 10323737
    [TBL] [Abstract][Full Text] [Related]  

  • 72. De novo partial duplication of 3q and distal deletion of 20p in a 15-week abort us with omphalocele.
    Cinti R; Botta G; Asnaghi V; Del Monaco A; Salvego M; Silengo M
    Fetal Diagn Ther; 2000; 15(1):61-2. PubMed ID: 10705217
    [No Abstract]   [Full Text] [Related]  

  • 73. Partial duplication 16q: report of two affected siblings resulting from a maternal translocation and literature review.
    Hahm SY; Chitayat D; Iqbal MA; Cho S; Nitowsky HM
    Clin Genet; 1987 May; 31(5):343-8. PubMed ID: 3301092
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Interstitial deletion 13q33 resulting from maternal insertional translocation.
    Emanuel BS; Zackai EH; Moreau L; Coates P; Orrechio E
    Clin Genet; 1979 Nov; 16(5):340-6. PubMed ID: 293234
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Early urethral obstruction sequence and unbalanced translocation with terminal 10p duplication/1p deficiency.
    Fryns JP; Vandenberghe K; Deschrijver D
    Genet Couns; 1997; 8(4):349-50. PubMed ID: 9457507
    [No Abstract]   [Full Text] [Related]  

  • 76. Disruption of a synaptotagmin (SYT14) associated with neurodevelopmental abnormalities.
    Quintero-Rivera F; Chan A; Donovan DJ; Gusella JF; Ligon AH
    Am J Med Genet A; 2007 Mar; 143A(6):558-63. PubMed ID: 17304550
    [TBL] [Abstract][Full Text] [Related]  

  • 77. A child with partial monosomy 6q secondary to a maternal direct insertional event.
    Matkins SV; Meyer JE; Berry AC
    J Med Genet; 1987 Apr; 24(4):227-9. PubMed ID: 3585939
    [TBL] [Abstract][Full Text] [Related]  

  • 78. 46,XY,der(3)t(1;3)(q23;p22): double aneuploidy at a new breakpoint.
    Joshi SN; Ganesh A; Venugopalan P
    Clin Dysmorphol; 2002 Apr; 11(2):145-6. PubMed ID: 12002149
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Uniparental isodisomy resulting from 46,XX,i(1p),i(1q) in a woman with short stature, ptosis, micro/retrognathia, myopathy, deafness, and sterility.
    Chen H; Young R; Mu X; Nandi K; Miao S; Prouty L; Ursin S; Gonzalez J; Yanamandra K
    Am J Med Genet; 1999 Jan; 82(3):215-8. PubMed ID: 10215543
    [TBL] [Abstract][Full Text] [Related]  

  • 80. An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region.
    Cremers FP; Pfeiffer RA; van de Pol TJ; Hofker MH; Kruse TA; Wieringa B; Ropers HH
    Hum Genet; 1987 Sep; 77(1):23-7. PubMed ID: 3476455
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.