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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

217 related items for PubMed ID: 31044557

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  • 28. Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex.
    Qi L, Wang M, Yagnik G, Mattheisen M, Gearhart JP, Lakshmanan Y, Ebert AK, Rösch W, Ludwig M, Draaken M, Reutter H, Boyadjiev SA.
    Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):759-63. PubMed ID: 23913486
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  • 30. Bladder exstrophy and epispadias complex in sibling: case report and review of literature.
    Kajbafzadeh AM, Tajik P, Payabvash S, Farzan S, Solhpour AR.
    Pediatr Surg Int; 2006 Sep; 22(9):767-70. PubMed ID: 16896811
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  • 33. 22q11.2 Microduplication with thyroid hemiagenesis.
    Kim HJ, Jo HS, Yoo EG, Chung IH, Kim SW, Lee KH, Chang YH.
    Horm Res Paediatr; 2013 Sep; 79(4):243-9. PubMed ID: 23364243
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  • 34. Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
    Draaken M, Reutter H, Schramm C, Bartels E, Boemers TM, Ebert AK, Rösch W, Schröder A, Stein R, Moebus S, Stienen D, Hoffmann P, Nöthen MM, Ludwig M.
    Eur J Med Genet; 2010 Sep; 53(2):55-60. PubMed ID: 20060941
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  • 37. Distal 22q11.2 microduplication combined with typical 22q11.2 proximal deletion: a case report.
    Molck MC, Vieira TP, Simioni M, Sgardioli IC, dos Santos AP, Xavier AC, Gil-da-Silva-Lopes VL.
    Am J Med Genet A; 2015 Jan; 167A(1):215-20. PubMed ID: 25358462
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  • 38. Is 1p36 deletion associated with anterior body wall defects?
    Çöllü M, Yüksel Ş, Şirin BK, Abbasoğlu L, Alanay Y.
    Am J Med Genet A; 2016 Jul; 170(7):1889-94. PubMed ID: 27144803
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  • 40. Bladder exstrophy-epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients.
    Reutter H, Thauvin-Robinet C, Boemers TM, Rösch WH, Ludwig M.
    Scand J Urol Nephrol; 2006 Jul; 40(3):221-4. PubMed ID: 16809264
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