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Human Genetics|November 1, 1990
Maternal transmission of ring chromosome 21I Kennerknecht, G Barbi, W VogelAmerican Journal of Medical Genetics|July 1, 1992
Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p)G Barbi, I Kennerknecht, C KlettAnnales De Genetique|January 1, 1984
Familial paracentric inversion inv(3)(q21q25.1). Case report and review of the literatureM Djalali, P Steinbach, G BarbiHuman Genetics|January 1, 1984
Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sitesG Barbi, P Steinbach, W VogelPrenatal Diagnosis|June 1, 1991
Mosaic trisomy 17 in amniotic fluid cells not confirmed in the newbornM Djalali, G Barbi, D GrabHuman Genetics|January 1, 1982
On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expressionP Steinbach, G Barbi, T BöllerMinerva Medica|February 25, 1980
[Spectrophotofluorimetric enzymatic determination of total serum bile acids]G Annoni, G Barbi, G BenzioAmerican Journal of Medical Genetics|December 1, 1993
Dup(1q)(q42-->qter) syndrome: case report and review of literatureI Kennerknecht, G Barbi, K RodensOphthalmic Genetics|March 1, 1994
Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13qI Kennerknecht, G Barbi, J GreherPageof 6