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Partial Monosomy 21 Associated with Unbalanced t(10p;21q)
Bon Su Koo, Sang Uk Park, Jae Hong Park, Su Yung Kim
Clin Exp Pediatr. 1995;38(8):1146-1150.   Published online August 15, 1995

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A case of monosomy 21 found to be an unbalanced de novo t(5p;21q) by fluorescence in situ hybridization
L. Flaherty, J. Moloney, N. Watson, L. Robson, L. Bousfield, A. Smith
Journal of Intellectual Disability Research. 2002;42(3):254-258   Crossref logo
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A case of presumptive monosomy 21 re-diagnosed as unbalanced t(5p;21q) by FISH and review of literature
M. Anwar Iqbal, Mohammed Zein Seid Ahmed, David Wu, Nadia Sakati
American Journal of Medical Genetics. 1997;70(2):174-178   Crossref logo
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Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21
M RIEGEL, P HARGREAVES, A BAUMER, M GUCSCEKIC, M IGNJATOVIC, A SCHINZEL
Annales de G�n�tique. 2004;   Crossref logo
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Unbalanced 13q/21q translocation: A revised study of the case previously reported as 21-monosomy
Tatsuro Ikeuchi, Ikuko Kondo, Motomichi Sasaki, Yasuhiko Kaneko, Susumu Kodama, Tsukasa Hattori
Human Genetics. 1976;33(3):327-330   Crossref logo
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Family with partial monosomy 10p and trisomy 10p
Ellis Hon, Cyril Chapman, Tania R. Gunn
American Journal of Medical Genetics. 1995;56(2):136-140   Crossref logo
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Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21
M. Riegel, P. Hargreaves, A. Baumer, M. Guc-Scekic, M. Ignjatovic, A. Schinzel
European Journal of Medical Genetics. 2005;48(2):167-174   Crossref logo
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Hypoparathyroidism with partial monosomy 10p
R. Koenig, R. Beetz
The Journal of Pediatrics. 1987;111(2):310   Crossref logo
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Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21
Birgitte Hertz, Carsten A. Brandt, Michael B. Petersen, Søren Pedersen, Ulrich König, Helle Strømkjaer, Peter K. A. Jensen
Clinical Genetics. 2008;44(2):89-94   Crossref logo
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Hypogammaglobulinemia and Silver-Russell phenotype associated with partial trisomy 7q and partial monosomy 21q
Hasibe Artac, Ismail Reisli, Mahmut Selman Yildirim, Gulseren Bagci, Guven Luleci, Orhan Hosgor, Sevim Karaaslan
American Journal of Medical Genetics Part A. 2009;149A(2):277-279   Crossref logo
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Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p
P. Lichtner, T. Attié-Bitach, S. Schuffenhauer, J. Henwood, P. Bouvagnet, P. Scambler, T. Meitinger, M. Vekemans
Journal of Molecular Medicine. 2002;80(7):431-442   Crossref logo
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