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Padiatrie Und Padologie|January 1, 1991
[Penoscrotal hypospadias with XXYY chromosome pattern]H Neugebauer, E Steichen-Gersdorf, J GlatzlClinical Dysmorphology|July 1, 1994
Oral-facial-digital syndrome II. Transitional type between Mohr and Majewski syndrome: report of a new case with congenital stenosis of the tracheaE Steichen-Gersdorf, I Gassner, B Covi, et al.Clinical Dysmorphology|April 1, 1997
Persistent hyperplastic primary vitreous in a family with osteoporosis-pseudoglioma syndromeE Steichen-Gersdorf, I Gassner, K Unsinn, et al.European Journal of Pediatrics|November 1, 1992
Familial cavernous angiomas of the brain: observations in a four generation familyE Steichen-Gersdorf, S Felber, W Fuchs, et al.British Journal of Cancer|January 1, 1997
Deletion mapping on chromosome 17p in medulloblastomaE Steichen-Gersdorf, M Baumgartner, A Kreczy, et al.Clinical Genetics|January 12, 2017
A recognizable type of syndromic short stature with arthrogryposis caused by bi-allelic SEMA3A loss-of-function variantsM Baumann, E Steichen-Gersdorf, B Krabichler, et al.Human Genetics|February 1, 1993
Hypomelanosis of Ito in a girl with plexus papilloma and translocation (X;17)E Steichen-Gersdorf, R Trawöger, H C Duba, et al.Journal of Inherited Metabolic Disease|January 1, 1994
A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rateW Sperl, G Bart, M T Vanier, et al.Clinical Genetics|July 12, 2008
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4E Steichen-Gersdorf, I Gassner, A Superti-Furga, et al.European Journal of Human Genetics : EJHG|March 1, 1997
Characterisation of X;17(q12;p13) translocation breakpoints in a female patient with hypomelanosis of Ito and choroid plexus papillomaV Zajac, T Kirchhoff, E R Levy, et al.Pageof 2