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G Schwanitz

Showing results (111-120 of 123) with videos related to

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Annales De Genetique|May 20, 2000
Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literatureS Mergenthaler, H A Wollmann, B Burger, et al.
Acta Neurologica Scandinavica|July 27, 2006
Global brain dysmyelination with above-average verbal skills in 18q- syndrome with a 17 Mb terminal deletionC Netzer, C Helmstaedter, A Ehrbrecht, et al.
American Journal of Medical Genetics|January 1, 1979
Distal 2q duplication: report of two familial cases and an attempt to define a syndromeM Zankl, G Schwanitz, P Schmid, et al.
Clinical Genetics|July 19, 2002
Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new casesKatja Eggermann, U A Mau, G Bujdosó, et al.
Human Genetics|May 1, 1996
Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typingT Eggermann, H Engels, B Moskalonek, et al.
Annales De Genetique|August 6, 1999
Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literatureT Eggermann, R Schubert, H Engels, et al.
Human Reproduction (Oxford, England)|September 2, 1999
Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injectionB Peschka, J Leygraaf, K Van der Ven, et al.
Molecular Human Reproduction|August 1, 1997
Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injectionK van der Ven, M Montag, B Peschka, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|May 16, 2002
Familial ovarian dysgerminomas (Swyer syndrome) in females associated with 46 XY-karyotypeA Kempe, H Engels, R Schubert, et al.
Journal of Medical Genetics|October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndromeB Horsthemke, A Maat-Kievit, E Sleegers, et al.
Pageof 13

Showing results (111-120 of 123) with videos related to

Sort By:
Pageof 13
Annales De Genetique|May 20, 2000
Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literatureS Mergenthaler, H A Wollmann, B Burger, et al.
Acta Neurologica Scandinavica|July 27, 2006
Global brain dysmyelination with above-average verbal skills in 18q- syndrome with a 17 Mb terminal deletionC Netzer, C Helmstaedter, A Ehrbrecht, et al.
American Journal of Medical Genetics|January 1, 1979
Distal 2q duplication: report of two familial cases and an attempt to define a syndromeM Zankl, G Schwanitz, P Schmid, et al.
Clinical Genetics|July 19, 2002
Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new casesKatja Eggermann, U A Mau, G Bujdosó, et al.
Human Genetics|May 1, 1996
Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typingT Eggermann, H Engels, B Moskalonek, et al.
Annales De Genetique|August 6, 1999
Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literatureT Eggermann, R Schubert, H Engels, et al.
Human Reproduction (Oxford, England)|September 2, 1999
Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injectionB Peschka, J Leygraaf, K Van der Ven, et al.
Molecular Human Reproduction|August 1, 1997
Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injectionK van der Ven, M Montag, B Peschka, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|May 16, 2002
Familial ovarian dysgerminomas (Swyer syndrome) in females associated with 46 XY-karyotypeA Kempe, H Engels, R Schubert, et al.
Journal of Medical Genetics|October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndromeB Horsthemke, A Maat-Kievit, E Sleegers, et al.
Pageof 13