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: 12244548)

  • 21. Duplication 3q syndrome: molecular delineation of the critical region.
    Aqua MS; Rizzu P; Lindsay EA; Shaffer LG; Zackai EH; Overhauser J; Baldini A
    Am J Med Genet; 1995 Jan; 55(1):33-7. PubMed ID: 7702094
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Duplication 9p and their implication to phenotype.
    Guilherme RS; Meloni VA; Perez AB; Pilla AL; de Ramos MA; Dantas AG; Takeno SS; Kulikowski LD; Melaragno MI
    BMC Med Genet; 2014 Dec; 15():142. PubMed ID: 25526829
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.
    Tsezou A; Kitsiou S; Galla A; Petersen MB; Karadima G; Syrrou M; Sahlèn S; Blennow E
    Am J Med Genet; 2000 Mar; 91(2):102-6. PubMed ID: 10748406
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.
    Matsuo M; Muroya K; Kosaki K; Ishii T; Fukushima Y; Anzo M; Ogata T
    Am J Med Genet; 1999 Sep; 86(1):44-50. PubMed ID: 10440827
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome.
    Loscalzo ML; Becker TA; Sutcliffe M
    Eur J Med Genet; 2008; 51(1):54-60. PubMed ID: 18006398
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Duplication of 8p23.2: a benign cytogenetic variant?
    Harada N; Takano J; Kondoh T; Ohashi H; Hasegawa T; Sugawara H; Ida T; Yoshiura K; Ohta T; Kishino T; Kajii T; Niikawa N; Matsumoto N
    Am J Med Genet; 2002 Aug; 111(3):285-8. PubMed ID: 12210324
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.
    Phelan MC; Stevenson RE; Anderson EV
    Am J Med Genet; 1993 May; 46(3):304-8. PubMed ID: 8488876
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism.
    Solomon NM; Nouri S; Warne GL; Lagerström-Fermér M; Forrest SM; Thomas PQ
    Genomics; 2002 Apr; 79(4):553-9. PubMed ID: 11944988
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
    Liehr T; Stumm M; Wegner RD; Bhatt S; Hickmann P; Patsalis PC; Meins M; Morlot S; Klaschka V; Ewers E; Hinreiner S; Mrasek K; Kosyakova N; Cai WW; Cheung SW; Weise A
    Cytogenet Genome Res; 2009; 124(1):102-5. PubMed ID: 19372675
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pure familial 6q21q22.1 duplication in two generations.
    Pazooki M; Lebbar A; Roubergues A; Baverel F; Letessier D; Dupont JM
    Eur J Med Genet; 2007; 50(1):60-5. PubMed ID: 17071147
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
    de Azevedo Moreira LM; Freitas LM; Gusmão FA; Riegel M
    Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):985-8. PubMed ID: 14745919
    [TBL] [Abstract][Full Text] [Related]  

  • 32. U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements.
    Rowe LR; Lee JY; Rector L; Kaminsky EB; Brothman AR; Martin CL; South ST
    J Med Genet; 2009 Oct; 46(10):694-702. PubMed ID: 19293169
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
    Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K
    Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151
    [TBL] [Abstract][Full Text] [Related]  

  • 34. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
    Hermsen MA; Tijssen M; Acero IH; Meijer GA; Ylstra B; Toral JF
    Eur J Med Genet; 2005; 48(3):310-8. PubMed ID: 16179226
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl with 46,XX,inv(7)dn karyotype and phenotypic abnormalities.
    Morales C; Mademont-Soler I; Armengol L; Milà M; Badenas C; Andrés S; Soler A; Sánchez A
    Cytogenet Genome Res; 2009; 125(4):334-40. PubMed ID: 19864897
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical variability of the 22q11.2 duplication syndrome.
    Wentzel C; Fernström M; Ohrner Y; Annerén G; Thuresson AC
    Eur J Med Genet; 2008; 51(6):501-10. PubMed ID: 18707033
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.
    Abu-Amero KK; Hellani AM; Salih MA; Seidahmed MZ; Elmalik TS; Zidan G; Bosley TM
    BMC Med Genet; 2010 Sep; 11():135. PubMed ID: 20858261
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
    Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
    Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Karyotype-phenotype analysis: 9p deletion versus 10q2 duplication.
    Hoo JJ
    Ann Genet; 1986; 29(4):266-8. PubMed ID: 3495230
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.
    Li Z; Yu T; Morishima M; Pao A; LaDuca J; Conroy J; Nowak N; Matsui S; Shiraishi I; Yu YE
    Hum Mol Genet; 2007 Jun; 16(11):1359-66. PubMed ID: 17412756
    [TBL] [Abstract][Full Text] [Related]  

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