FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome von Catrinel Marinescu, R, Johnson, Elizabeth I, Grady, Deborah, Chen, Xiao-Ning, Overhauser, Joan

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Hemizygosity of δ-Catenin (CTNND2) Is Associated with Severe Mental Retardation in Cri-du-Chat Syndrome von Medina, Miguel, Marinescu, R.Catrinel, Overhauser, Joan, Kosik, Kenneth S.

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5p14 deletion associated with microcephaly and seizures von Johnson, Elizabeth I, Marinescu, R Catrinel, Punnett, Hope H, Tenenholz, Beverly, Overhauser, Joan

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No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndrome von Marinescu, R. Catrinel, Johnson, Elizabeth I., Dykens, Elisabeth M., Hodapp, Robert M., Overhauser, Joan

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Variability in a family with an insertion involving 5p von Marinescu, R. Catrinel, Mamunes, Peter, Kline, Antonie D., Schmidt, Jennifer, Rojas, Katherine, Overhauser, Joan

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Exclusion of the gene for human cartilage intermediate layer protein in currently mapped calcium pyrophosphate dihydrate deposition syndromes von Marinescu, R. Catrinel, Nyce, Kristin, De La Peñaa, Lourdes Serrano, Overhauser, Joan, Williams, Charlene J.

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Growth charts for cri-du-chat syndrome: An international collaborative study von Marinescu, R. Catrinel, Mainardi, Paola Cerruti, Collins, Margaret Ross, Kouahou, Martine, Coucourde, Gabriella, Pastore, Guido, Eaton-Evans, Jill, Overhauser, Joan

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Human exonuclease I interacts with the mismatch repair protein hMSH2 von SCHMUTTE, C, MARINESCU, R. C, SADOFF, M. M, GUERRETTE, S, OVERHAUSER, J, FISHEL, R

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Refined chromosomal localization of the mismatch repair and hereditary nonpolyposis colorectal cancer genes hMSH2 and hMSH6 von SCHMUTTE, C, MARINESCU, R. C, COPELAND, N. G, JENKINS, N. A, OVERHAUSER, J, FISHEL, R

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