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Journal Abstract Search

135 related items for PubMed ID: 16001439

  • 21. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M, Hwu WL, Kuo SJ, Chen CP, Yin PL, Chang SP, Lee DJ, Chen TH, Wang BT, Lin CC.
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
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  • 22. Phenotypic variability of atypical 22q11.2 deletions not including TBX1.
    Verhagen JM, Diderich KE, Oudesluijs G, Mancini GM, Eggink AJ, Verkleij-Hagoort AC, Groenenberg IA, Willems PJ, du Plessis FA, de Man SA, Srebniak MI, van Opstal D, Hulsman LO, van Zutven LJ, Wessels MW.
    Am J Med Genet A; 2012 Oct; 158A(10):2412-20. PubMed ID: 22893440
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  • 23. Increased prevalence of unprovoked seizures in patients with a 22q11.2 deletion.
    Kao A, Mariani J, McDonald-McGinn DM, Maisenbacher MK, Brooks-Kayal AR, Zackai EH, Lynch DR.
    Am J Med Genet A; 2004 Aug 15; 129A(1):29-34. PubMed ID: 15266612
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  • 24. Frequent association of 22q11.2 deletion with tetralogy of Fallot.
    Maeda J, Yamagishi H, Matsuoka R, Ishihara J, Tokumura M, Fukushima H, Ueda H, Takahashi E, Yoshiba S, Kojima Y.
    Am J Med Genet; 2000 Jun 05; 92(4):269-72. PubMed ID: 10842294
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  • 25. Polymicrogyria in chromosome 22q11 deletion syndrome.
    Ghariani S, Dahan K, Saint-Martin C, Kadhim H, Morsomme F, Moniotte S, Verellen-Dumoulin C, Sébire G.
    Eur J Paediatr Neurol; 2002 Jun 05; 6(1):73-7. PubMed ID: 11993959
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  • 27. Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome.
    Ockeloen CW, de Leeuw N, Mieloo H, Reijnen IGM, de Vries BBA.
    Clin Dysmorphol; 2010 Jul 05; 19(3):137-139. PubMed ID: 20357662
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  • 31. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.
    Pathologica; 1999 Jun 05; 91(3):166-72. PubMed ID: 10536461
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  • 32. Deletion 22q11 in patients with interrupted aortic arch.
    Marino B, Digilio MC, Persiani M, Di Donato R, Toscano A, Giannotti A, Dallapiccola B.
    Am J Cardiol; 1999 Aug 01; 84(3):360-1, A9. PubMed ID: 10496456
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  • 33. Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndrome.
    Yamamoto T, Sameshima K, Sekido K, Aida N, Matsumoto N, Naritomi K, Kurosawa K.
    Am J Med Genet A; 2006 Jun 15; 140(12):1302-4. PubMed ID: 16691595
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  • 37. Schizophrenia and hypocalcaemia: variable phenotype of deletion at chromosome 22q911.
    Chow LY, Garcia-Barcelo M, Wing YK, Waye MM.
    Aust N Z J Psychiatry; 1999 Oct 15; 33(5):760-2. PubMed ID: 10545003
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  • 38. A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21.
    Motegi T, Ohuchi M, Ohtaki C, Fujiwara K, Enomoto S, Hasegawa T, Kishi K, Hayakawa H.
    Hum Genet; 1985 Oct 15; 71(2):160-2. PubMed ID: 4043965
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  • 39. Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome.
    Sakamoto O, Imaizumi M, Suzuki A, Sato A, Tanaka T, Ogawa E, Kumaki S, Iinuma K.
    Pediatr Int; 2004 Oct 15; 46(5):612-4. PubMed ID: 15491395
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