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American Journal of Medical Genetics. Part A
|
February 14, 2006
Healthy 12-year-old boy with mosaic inv dup(15)(q13)
Anne Loitzsch, Oliver Bartsch
American Journal of Medical Genetics. Part A
|
January 22, 2004
Retinoblastoma, pinealoma, and mild overgrowth in a boy with a deletion of RB1 and neighbor genes on chromosome 13q14
Cristina Skrypnyk, Oliver Bartsch
Clinical Dysmorphology
|
February 17, 2016
A recurrent TP63 mutation causing EEC3 and Rapp-Hodgkin syndromes
Felix B Brueggemann, Oliver Bartsch
FEBS Letters
|
August 5, 2008
Only plant-type (GLYK) glycerate kinases produce d-glycerate 3-phosphate
Oliver Bartsch, Martin Hagemann, Hermann Bauwe
Journal of Applied Genetics
|
April 6, 2011
Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism
Ruth Mikelsaar, Jelena Lissitsina, Oliver Bartsch
American Journal of Medical Genetics. Part A
|
March 29, 2005
A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome
Katrin Ounap, Tiiu Ilus, Oliver Bartsch
European Journal of Pediatrics
|
December 4, 2009
Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism
Jutta Jenderny, Winfried Schmidt, Oliver Bartsch
American Journal of Medical Genetics. Part A
|
July 3, 2003
Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype?
Dagmar Wieczorek, Oliver Bartsch, Gabriele Gillessen-Kaesbach
European Journal of Human Genetics : EJHG
|
March 10, 2005
FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22)
Oliver Bartsch, Sasan Rasi, Kristina Hoffmann, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
Novel clinical findings in the first Egyptian case of Sotos syndrome caused by complete deletion of the NSD1 gene
Ebtesam Abdalla, Oliver Bartsch, Danuta Galetzka, et al.
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of 12
Search research articles
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Showing results (1-10 of 118) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics. Part A
|
February 14, 2006
Healthy 12-year-old boy with mosaic inv dup(15)(q13)
Anne Loitzsch, Oliver Bartsch
American Journal of Medical Genetics. Part A
|
January 22, 2004
Retinoblastoma, pinealoma, and mild overgrowth in a boy with a deletion of RB1 and neighbor genes on chromosome 13q14
Cristina Skrypnyk, Oliver Bartsch
Clinical Dysmorphology
|
February 17, 2016
A recurrent TP63 mutation causing EEC3 and Rapp-Hodgkin syndromes
Felix B Brueggemann, Oliver Bartsch
FEBS Letters
|
August 5, 2008
Only plant-type (GLYK) glycerate kinases produce d-glycerate 3-phosphate
Oliver Bartsch, Martin Hagemann, Hermann Bauwe
Journal of Applied Genetics
|
April 6, 2011
Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism
Ruth Mikelsaar, Jelena Lissitsina, Oliver Bartsch
American Journal of Medical Genetics. Part A
|
March 29, 2005
A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome
Katrin Ounap, Tiiu Ilus, Oliver Bartsch
European Journal of Pediatrics
|
December 4, 2009
Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism
Jutta Jenderny, Winfried Schmidt, Oliver Bartsch
American Journal of Medical Genetics. Part A
|
July 3, 2003
Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype?
Dagmar Wieczorek, Oliver Bartsch, Gabriele Gillessen-Kaesbach
European Journal of Human Genetics : EJHG
|
March 10, 2005
FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22)
Oliver Bartsch, Sasan Rasi, Kristina Hoffmann, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
Novel clinical findings in the first Egyptian case of Sotos syndrome caused by complete deletion of the NSD1 gene
Ebtesam Abdalla, Oliver Bartsch, Danuta Galetzka, et al.
Page
of 12