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Clinical Genetics|January 15, 2000
FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndromeR C Marinescu, E I Johnson, D Grady, et al.American Journal of Human Genetics|December 1, 1993
Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18R Mewar, A D Kline, W Harrison, et al.Human Molecular Genetics|February 1, 1995
Five novel genes from the cri-du-chat critical region isolated by direct selectionA D Simmons, S A Goodart, T D Gallardo, et al.Genomics|February 1, 1993
STS map of genes and anonymous DNA fragments on human chromosome 18 using a panel of somatic cell hybridsJ Overhauser, R Mewar, K Rojas, et al.American Journal of Medical Genetics|August 15, 1994
Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotypeR Mewar, W Harrison, D D Weaver, et al.Cancer Research|October 27, 1998
Human exonuclease I interacts with the mismatch repair protein hMSH2C Schmutte, R C Marinescu, M M Sadoff, et al.American Journal of Medical Genetics|August 10, 1999
No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndromeR C Marinescu, E I Johnson, E M Dykens, et al.American Journal of Medical Genetics|September 14, 1999
Variability in a family with an insertion involving 5pR C Marinescu, P Mamunes, A D Kline, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1984
Transformation properties of type 5 adenovirus mutants that differentially express the E1A gene productsK P Haley, J Overhauser, L E Babiss, et al.American Journal of Medical Genetics|October 1, 1992
Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5L D Keppen, S M Gollin, D Edwards, et al.Pageof 8