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Dagmar Wieczorek

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|November 22, 2018
Autosomal dominant intellectual disabilityDagmar Wieczorek
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 10, 2024
Syndromology at the interface of evolving phenotypes, epimutations, and model systemsNuria C Bramswig, Dagmar Wieczorek
American Journal of Medical Genetics. Part A|October 6, 2006
Oculo-oto-facial dysplasia (OOFD) versus Burn-McKeown syndromeDagmar Wieczorek, Gabriele Gillessen-Kaesbach
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 10, 2024
Implementation of human genetic counseling in the MZEB (Medical Center for Adults with disabilities) at the psychiatric LVR Clinic Bedburg-HauDorothee Maliszewski-Makowka, Dagmar Wieczorek
Seminars in Fetal & Neonatal Medicine|September 25, 2021
Genetics of craniofacial malformationsAriane Schmetz, Jeanne Amiel, Dagmar Wieczorek
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
American Journal of Medical Genetics|March 14, 2002
Absence of thumbs, A/hypoplasia of radius, hypoplasia of ulnae, retarded bone age, short stature, microcephaly, hypoplastic genitalia, and mental retardationDagmar Wieczorek, Bernhard Köster, Gabriele Gillessen-Kaesbach
Molecular and Cellular Pediatrics|October 7, 2017
Autism spectrum disorder and Li-Fraumeni syndrome: purely coincidental or mechanistically associated?Michaela Kuhlen, Julia Taeubner, Dagmar Wieczorek, et al.
Pediatric Blood & Cancer|July 26, 2019
How I approach hereditary cancer predisposition in a child with cancerMichaela Kuhlen, Dagmar Wieczorek, Reiner Siebert, et al.
European Journal of Medical Genetics|August 30, 2008
Left-ventricular non-compaction (LVNC): a clinical feature more often observed in terminal deletion 1p36 than previously expectedKirsten Cremer, Hermann-Josef Lüdecke, Frauke Ruhr, et al.
Pageof 25

Showing results (1-10 of 250) with videos related to

Sort By:
Pageof 25
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|November 22, 2018
Autosomal dominant intellectual disabilityDagmar Wieczorek
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 10, 2024
Syndromology at the interface of evolving phenotypes, epimutations, and model systemsNuria C Bramswig, Dagmar Wieczorek
American Journal of Medical Genetics. Part A|October 6, 2006
Oculo-oto-facial dysplasia (OOFD) versus Burn-McKeown syndromeDagmar Wieczorek, Gabriele Gillessen-Kaesbach
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 10, 2024
Implementation of human genetic counseling in the MZEB (Medical Center for Adults with disabilities) at the psychiatric LVR Clinic Bedburg-HauDorothee Maliszewski-Makowka, Dagmar Wieczorek
Seminars in Fetal & Neonatal Medicine|September 25, 2021
Genetics of craniofacial malformationsAriane Schmetz, Jeanne Amiel, Dagmar Wieczorek
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
American Journal of Medical Genetics|March 14, 2002
Absence of thumbs, A/hypoplasia of radius, hypoplasia of ulnae, retarded bone age, short stature, microcephaly, hypoplastic genitalia, and mental retardationDagmar Wieczorek, Bernhard Köster, Gabriele Gillessen-Kaesbach
Molecular and Cellular Pediatrics|October 7, 2017
Autism spectrum disorder and Li-Fraumeni syndrome: purely coincidental or mechanistically associated?Michaela Kuhlen, Julia Taeubner, Dagmar Wieczorek, et al.
Pediatric Blood & Cancer|July 26, 2019
How I approach hereditary cancer predisposition in a child with cancerMichaela Kuhlen, Dagmar Wieczorek, Reiner Siebert, et al.
European Journal of Medical Genetics|August 30, 2008
Left-ventricular non-compaction (LVNC): a clinical feature more often observed in terminal deletion 1p36 than previously expectedKirsten Cremer, Hermann-Josef Lüdecke, Frauke Ruhr, et al.
Pageof 25