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Journal Abstract Search

130 related items for PubMed ID: 18444226

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  • 22. [Application of array comparative genomic hybridization in prenatal diagnosis of a case with 5q35 deletion syndrome].
    Feng Z, Hu H, Mao C, Wang D, Liu L, Liu S, Jing Z, Liu H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr 10; 34(2):240-243. PubMed ID: 28397228
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  • 23. Radiological features of the most common autosomal disorders: trisomy 21-22 (mongolism or Down's syndrome), trisomy 18, trisomy 13-15, and the cri du chat syndrome.
    James AE, Merz T, Janower ML, Dorst JP.
    Clin Radiol; 1971 Oct 10; 22(4):417-33. PubMed ID: 4257566
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  • 24. Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition.
    Kjaer I, Niebuhr E.
    Am J Med Genet; 1999 Jan 01; 82(1):6-14. PubMed ID: 9916835
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  • 30. Parental origin of chromosome 5 deletions in the cri-du-chat syndrome.
    Overhauser J, McMahon J, Oberlender S, Carlin ME, Niebuhr E, Wasmuth JJ, Lee-Chen J.
    Am J Med Genet; 1990 Sep 01; 37(1):83-6. PubMed ID: 1978567
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