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Journal Abstract Search

348 related items for PubMed ID: 25297596

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  • 22. 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; 91(3):166-72. PubMed ID: 10536461
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  • 23. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
    Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A.
    Am J Med Genet; 1995 Jul 03; 57(3):514-22. PubMed ID: 7677167
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  • 28. The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system.
    Mikhail FM, Burnside RD, Rush B, Ibrahim J, Godshalk R, Rutledge SL, Robin NH, Descartes MD, Carroll AJ.
    Genet Med; 2014 Jan 03; 16(1):92-100. PubMed ID: 23765049
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  • 29. Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.
    Shetty M, Srikanth A, Kadandale J, Hegde S.
    Cytogenet Genome Res; 2016 Jan 03; 148(4):249-55. PubMed ID: 27300488
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  • 33. The 22q11.2 deletion syndrome.
    Emanuel BS, McDonald-McGinn D, Saitta SC, Zackai EH.
    Adv Pediatr; 2001 Jan 03; 48():39-73. PubMed ID: 11480765
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  • 37. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.
    Ophthalmic Genet; 2014 Dec 03; 35(4):248-51. PubMed ID: 23834556
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  • 38. Atypical 581-kb 22q11.21 Deletion in a Patient with Oculo-Auriculo-Vertebral Spectrum Phenotype.
    Colovati ME, Bragagnolo S, Guilherme RS, Dantas AG, Soares MF, Kim CA, Perez AB, Melaragno MI.
    Cytogenet Genome Res; 2015 Dec 03; 147(2-3):130-4. PubMed ID: 26919065
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  • 39. [Genotype and phenotype analysis of two patients with Williams syndrome].
    Zhu H, Ji C, Zhang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb 03; 33(1):68-70. PubMed ID: 26829738
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  • 40. [Prenatal diagnosis of 22q11.2 microdeletion by multiplex ligation-dependent probe amplification].
    Luo CY, Ma DY, Zhang JJ, Hu P, Cao L, Ji XQ, Zhou J, Liu A, Wu Y, Cheng J, Lin Y, Xu ZF.
    Zhonghua Fu Chan Ke Za Zhi; 2013 Nov 03; 48(11):824-7. PubMed ID: 24444558
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