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Journal Abstract Search

141 related items for PubMed ID: 15690381

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  • 6. Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype.
    Ewing AD, Cheetham SW, McGill JJ, Sharkey M, Walker R, West JA, West MJ, Summers KM.
    Am J Med Genet A; 2021 Jul; 185(7):2070-2083. PubMed ID: 33960642
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  • 7. [A nevoid basal cell carcinoma syndrome with chromosomal aberration].
    Sasaki K, Yoshimoto T, Nakao T, Minagawa K, Takahashi Y, Watanabe Y, Tanabe C.
    No To Hattatsu; 2000 Jan; 32(1):49-55. PubMed ID: 10655752
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  • 8. Gorlin syndrome patient with large deletion in 9q22.32-q22.33 detected by quantitative multiplex fluorescent PCR.
    Musani V, Cretnik M, Situm M, Basta-Juzbasic A, Levanat S.
    Dermatology; 2009 Jan; 219(2):111-8. PubMed ID: 19439922
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  • 9. Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts.
    Lench NJ, High AS, Markham AF, Hume WJ, Robinson PA.
    Eur J Cancer B Oral Oncol; 1996 May; 32B(3):202-6. PubMed ID: 8762878
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  • 11. A girl with deletion 9q22.1-q22.32 including the PTCH and ROR2 genes identified by genome-wide array-CGH.
    Nowakowska B, Kutkowska-Kaźmierczak A, Stankiewicz P, Bocian E, Obersztyn E, Ou Z, Cheung SW, Cai WW.
    Am J Med Genet A; 2007 Aug 15; 143A(16):1885-9. PubMed ID: 17632781
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  • 12. Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients.
    Bonifas JM, Bare JW, Kerschmann RL, Master SP, Epstein EH.
    Hum Mol Genet; 1994 Mar 15; 3(3):447-8. PubMed ID: 8012356
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  • 13. Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.
    Olivieri C, Maraschio P, Caselli D, Martini C, Beluffi G, Maserati E, Danesino C.
    Eur J Pediatr; 2003 Feb 15; 162(2):100-3. PubMed ID: 12548386
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  • 15. NBCCS secondary to an interstitial chromosome 9q deletion.
    Haniffa MA, Leech SN, Lynch SA, Simpson NB.
    Clin Exp Dermatol; 2004 Sep 15; 29(5):542-4. PubMed ID: 15347344
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  • 16. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.
    Muller EA, Aradhya S, Atkin JF, Carmany EP, Elliott AM, Chudley AE, Clark RD, Everman DB, Garner S, Hall BD, Herman GE, Kivuva E, Ramanathan S, Stevenson DA, Stockton DW, Hudgins L.
    Am J Med Genet A; 2012 Feb 15; 158A(2):391-9. PubMed ID: 22190277
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  • 17. Novel mutations in the PATCHED gene in basal cell nevus syndrome.
    Lam CW, Leung CY, Lee KC, Xie J, Lo FM, Au TS, Tong SF, Poon MK, Chan LY, Luk NM.
    Mol Genet Metab; 2002 May 15; 76(1):57-61. PubMed ID: 12175781
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  • 19. Destructive basal cell carcinoma in a patient with basal cell nevus syndrome and an interstitial deletion of chromosome 9q22.
    Mosterd K, Sommer A, van Marion A, Lacko M, Herbergs J, de Bondt BJ, van Steensel MA, Kelleners-Smeets NW.
    Dermatol Surg; 2009 Dec 15; 35(12):2051-3. PubMed ID: 20050151
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