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Prenatal Diagnosis|July 1, 1991
Post-mortem findings in a fetus with 48,XXY,+21A Smith, G Watson, J Michas, et al.American Journal of Medical Genetics|September 15, 1991
Ring chromosome 15 and 15qs+ mosaic: clinical and cytogenetic behaviour spanning 29 yearsA Smith, G den Dulk, R Viersbach, et al.American Journal of Medical Genetics|June 13, 1997
Identification of supernumerary der(20) chromosomes by FISH in three patientsR Viersbach, H Engels, G SchwanitzThe Australian & New Zealand Journal of Obstetrics & Gynaecology|August 1, 1990
Cytogenetic studies in perinatal deathA Smith, P Bannatyne, P Russell, et al.Human Genetics|June 1, 1994
Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomesR Viersbach, G Schwanitz, M M NöthenAmerican Journal of Medical Genetics|April 17, 1998
Delineation of supernumerary marker chromosomes in 38 patientsR Viersbach, H Engels, U Gamerdinger, et al.American Journal of Medical Genetics|September 19, 1997
Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selectionR Schubert, R Viersbach, T Eggermann, et al.Journal of Medical Genetics|July 25, 1998
Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibsD Wieczorek, H Engels, R Viersbach, et al.The Australian & New Zealand Journal of Obstetrics & Gynaecology|November 1, 1991
Amniocentesis in the management of preterm premature rupture of the membranesJ Dudley, G Malcolm, D EllwoodPrenatal Diagnosis|May 1, 1995
Amniotic alpha-fetoprotein in the prenatal diagnosis of congenital nephrotic syndrome of the Finnish typeJ Morris, D Ellwood, D Kennedy, et al.Pageof 2,077