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TOP 3
E Back; R Toder; A Fuchshuber
De novo inverted duplication of chromosome 7(q21.3-->q35): cytogenetic diagnosis confirmed by FISH analysis.
Jutta Wirth; E Back; Alexander Hüttenhofer; Hans Gerd Nothwang; Christina Lich; Stephanie Gross; Corinna Menzel; A Schinzel; P Kioschis; Niels Tommerup; Hans-Hilger Ropers; Bernhard Horsthemke; Karin Buiting
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15.
Dietmar Pfeifer; Ralf Kist; Ken Dewar; KL Devon; Eric S Lander; Bruce Birren; L Korniszewski; E Back; Gerd Scherer
Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region.

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All Publications

2001: E Back; R Toder; A Fuchshuber
De novo inverted duplication of chromosome 7(q21.3-->q35): cytogenetic diagnosis confirmed by FISH analysis.
Clinical genetics 2001;60(1):77-82.
2001: Jutta Wirth; E Back; Alexander Hüttenhofer; Hans Gerd Nothwang; Christina Lich; Stephanie Gross; Corinna Menzel; A Schinzel; P Kioschis; Niels Tommerup; Hans-Hilger Ropers; Bernhard Horsthemke; Karin Buiting
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15.
Human molecular genetics 2001;10(3):201-10.
1999: Dietmar Pfeifer; Ralf Kist; Ken Dewar; KL Devon; Eric S Lander; Bruce Birren; L Korniszewski; E Back; Gerd Scherer
Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region.
American journal of human genetics 1999;65(1):111-24.
1997: E Back; W Kratzer; S Zeitler; Werner Schempp
De novo duplication of 12pter-->p12.1: clinical and cytogenetic diagnosis confirmed by chromosome painting.
Clinical genetics 1997;51(3):205-10.
1997: T Wagner; Niels Tommerup; Jutta Wirth; H Leffers; J Zimmer; E Back; J Weissenbach; Gerd Scherer
A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3.
Cytogenetics and cell genetics 1997;76(3-4):172-5.
1997: E Back; C Jung; S Zeitler; Werner Schempp
De novo duplication of 7pter-->p21.2 and deletion of 9pter-->p23.5: clinical and cytogenetic diagnosis.
Clinical genetics 1997;51(1):56-60.
1995: C Jung; G Wolff; E Back; M Stahl
Two unrelated children with developmental delay, short stature and anterior chamber cleavage disorder, cerebellar hypoplasia, endocrine disturbances and tracheostenosis: a new entity?
Clinical dysmorphology 1995;4(1):44-51.
1994: E Back; R Toder; I Voiculescu; A Wildberg; Werner Schempp
De novo isochromosome 18p in two patients: cytogenetic diagnosis and confirmation by chromosome painting.
Clinical genetics 1994;45(6):301-4.
1993: I Voiculescu; R Toder; E Back; P Osswald; Werner Schempp
A retrospective CISS hybridization analysis of a case with de novo translocation t(18;22) resulting in an 18p- syndrome.
Clinical genetics 1993;43(6):318-20.
1991: I Voiculescu; E Back; Werner Schempp
Homozygous condition for a BrdU-requiring fragile site on chromosome 12.
Human genetics 1991;86(4):416-7.
1989: E Back; I Voiculescu; M Brünger; G Wolff
Familial ring (20) chromosomal mosaicism.
Human genetics 1989;83(2):148-54.
1989: G Wolff; E Back; S Arleth; U Rapp-Körner
Genetic counseling in families with inherited balanced translocations: experience with 36 families.
Clinical genetics 1989;35(6):404-16.
1988: C Hausmann; E Back; G Wolff; I Voiculescu
Deletion 11q23.3 without familial predisposition.
Human genetics 1988;80(2):205.
1988: I Voiculescu; C Hausmann; G Wolff; E Back
A BrdU-requiring fragile site on chromosome 12.
Human genetics 1988;78(2):183-5.
1987: I Voiculescu; E Back; A M Duncan; H Schwaibold; Werner Schempp
Trisomy 22 in a newborn with multiple malformations.
Human genetics 1987;76(3):298-301.
1986: I Voiculescu; G Barbi; G Wolff; P Steinbach; E Back; Werner Schempp
Familial pericentric inversion of chromosome 12.
Human genetics 1986;72(4):320-2.