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Almuth Caliebe

Showing results (1-10 of 81) with videos related to

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European Journal of Medical Genetics|May 27, 2008
Catel-Manzke syndrome: two new patients and a critical review of the literatureHermann Manzke, Katarina Lehmann, Eva Klopocki, et al.
Movement Disorders Clinical Practice|October 27, 2018
The Co-Occurrence of Tricho-Rhino-Phalangeal Syndrome and Early-Onset Levodopa-Sensitive ParkinsonismFranziska Hopfner, Almuth Caliebe, Günther Deuschl, et al.
Archives of Gynecology and Obstetrics|March 2, 2018
Reply to letter by Dr. G. CorsoFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
Archives of Gynecology and Obstetrics|October 11, 2017
CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohortFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|April 7, 2015
Partial hydatidiform mole with extensive angiomatoid vessel configuration in a first trimester miscarriageHenning Feist, Almuth Caliebe, Jennifer Oates, et al.
European Journal of Medical Genetics|May 24, 2011
A de novo 0.57 Mb microdeletion in chromosome 11q13.1 in a patient with speech problems, autistic traits, dysmorphic features and multiple endocrine neoplasia type 1Inga Mohrmann, Gabriele Gillessen-Kaesbach, Reiner Siebert, et al.
American Journal of Medical Genetics. Part A|September 19, 2012
Growth retardation, intellectual disability, facial anomalies, cataract, thoracic hypoplasia, and skeletal abnormalities: a novel phenotypeHitesh Shah, Susanne Bens, Almuth Caliebe, et al.
European Journal of Pediatrics|November 9, 2002
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasiaEva Morava, Judit Kárteszi, János Weisenbach, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 12, 2011
Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18--how to counsel?Christel Eckmann-Scholz, Holger Tönnies, Thomas Liehr, et al.
BMC Genomics|November 18, 2025
Comprehensive androgen-dependent transcriptome analysis in human genital tissueRadhika Sivaprasad, Kristian Händler, Almuth Caliebe, et al.
Pageof 9

Showing results (1-10 of 81) with videos related to

Sort By:
Pageof 9
European Journal of Medical Genetics|May 27, 2008
Catel-Manzke syndrome: two new patients and a critical review of the literatureHermann Manzke, Katarina Lehmann, Eva Klopocki, et al.
Movement Disorders Clinical Practice|October 27, 2018
The Co-Occurrence of Tricho-Rhino-Phalangeal Syndrome and Early-Onset Levodopa-Sensitive ParkinsonismFranziska Hopfner, Almuth Caliebe, Günther Deuschl, et al.
Archives of Gynecology and Obstetrics|March 2, 2018
Reply to letter by Dr. G. CorsoFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
Archives of Gynecology and Obstetrics|October 11, 2017
CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohortFrederik Stuebs, Simone Heidemann, Almuth Caliebe, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|April 7, 2015
Partial hydatidiform mole with extensive angiomatoid vessel configuration in a first trimester miscarriageHenning Feist, Almuth Caliebe, Jennifer Oates, et al.
European Journal of Medical Genetics|May 24, 2011
A de novo 0.57 Mb microdeletion in chromosome 11q13.1 in a patient with speech problems, autistic traits, dysmorphic features and multiple endocrine neoplasia type 1Inga Mohrmann, Gabriele Gillessen-Kaesbach, Reiner Siebert, et al.
American Journal of Medical Genetics. Part A|September 19, 2012
Growth retardation, intellectual disability, facial anomalies, cataract, thoracic hypoplasia, and skeletal abnormalities: a novel phenotypeHitesh Shah, Susanne Bens, Almuth Caliebe, et al.
European Journal of Pediatrics|November 9, 2002
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasiaEva Morava, Judit Kárteszi, János Weisenbach, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 12, 2011
Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18--how to counsel?Christel Eckmann-Scholz, Holger Tönnies, Thomas Liehr, et al.
BMC Genomics|November 18, 2025
Comprehensive androgen-dependent transcriptome analysis in human genital tissueRadhika Sivaprasad, Kristian Händler, Almuth Caliebe, et al.
Pageof 9