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Human Genetics|June 1, 1996
A PCR-based test suitable for screening for fragile X syndrome among mentally retarded malesL A Haddad, R C Mingroni-Netto, A M Vianna-Morgante, et al.Journal of Medical Genetics|July 1, 1996
FRAXF in a patient with chromosome 8 duplicationA M Vianna-Morgante, R C Mingroni-Netto, A C Barbosa, et al.Cancer Genetics and Cytogenetics|January 1, 1995
Selection of adrenal tumor cells in culture demonstrated by interphase cytogeneticsC Rosenberg, V A Della-Rosa, A C Latronico, et al.American Journal of Medical Genetics|October 1, 1986
Duchenne muscular dystrophy in a girl with a 45,X/46,XX/47,XXX chromosome constitutionE R Bortolini, D M da Silva, R S Chequer, et al.Human Genetics|April 24, 1978
Partial monosomy 13 and 21 due to a familial 13/21 translocationP G Otto, S Toledo, A Richieri-Costa, et al.American Journal of Medical Genetics|October 23, 1995
Identification of a supernumerary marker derived from chromosome 17 using FISHC Rosenberg, C L Borovik, R S Canonaco, et al.Human Genetics|December 24, 1997
RB1 deletion in gonadoblastoma in an XY femaleS Antonini, A S Barbosa, C Rosenberg, et al.American Journal of Medical Genetics|July 31, 1995
Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12qC P Koiffmann, C H Gonzalez, A M Vianna-Morgante, et al.Journal of Medical Genetics|February 1, 1977
Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same familyR B Levisky, A M Vianna-Morgante, O Frota-Pessoa, et al.Clinical Genetics|February 11, 2012
PLP1 duplication at the breakpoint regions of an apparently balanced t(X;22) translocation causes Pelizaeus-Merzbacher disease in a girlA C S Fonseca, A Bonaldi, S S Costa, et al.Pageof 5