U
Uta Francke
Researcher at Stanford University
Publications - 475
Citations - 49980
Uta Francke is an academic researcher from Stanford University. The author has contributed to research in topics: Gene & Gene mapping. The author has an hindex of 108, co-authored 475 publications receiving 48481 citations. Previous affiliations of Uta Francke include McGill University & University of North Carolina at Chapel Hill.
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Journal ArticleDOI
Requirement of human chromosomes 19, 6 and possibly 3 for infection of hamster × human hybrid cells with baboon M7 type C virus
TL;DR: It is concluded that human chromosomes 6 and 19 code for functions involved in M7 virus metabolism, and the cannot exclude a function coded for by chromosome 3.
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Conserved autosomal syntenic group on mouse (MMU) chromosome 15 and human (HSA) chromosome 22: assignment of a gene for arylsulfatase A to MMU 15 and regional mapping of DIAl, ARSA, and ACO2 on HSA 22
TL;DR: Evidence for another syntenic relationship that has been conserved is found by regional mapping of human DIA1 and ARSA using somatic cell hybrids segregating a human chromosome translocation t(15;22)(q14;q13.31).
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Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy
Marten H. Hofker,A. A. B. Bergen,M. I. Skraastad,Egbert Bakker,Uta Francke,B. Wieringa,J A Bartley,G.J.B. van Ommen,Peter L. Pearson +8 more
TL;DR: A random cosmid cX5, isolated from this cosmid, identifies an MspI RFLP, with a minor allele frequency of 35%.
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Minute chromosomes replacing the Y chromosome carry Y-specific sequences by restriction fragment analysis and in situ hybridization.
Maximilian Munke,Bérengère de Martinville,Uta Francke,Ernest Lieber,John M. Opitz,James F. Reynolds +5 more
TL;DR: Two unrelated males, a 43- year-old man with azoospermia and a 4-year-old boy with stature at the 10th centile, had similar karyotypes: 46,X,min; molecular techniques showed that these sequences were present on the minute chromosomes and have not been translocated elsewhere.
Journal ArticleDOI
Partial trisomy 20p derived from a t(18;20) translocation
Kenneth M. Taylor,Kenneth M. Taylor,Howard L. Wolfinger,Michael G. Brown,Michael G. Brown,David L. Chadwick,Uta Francke +6 more
TL;DR: Two sibs show a strikingly concordant syndrome of congenital anomalies and G-banding reveals that each has partial trisomy 20p resulting from a t(18;20) translocation.