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Clinical Dysmorphology|August 24, 2000
SOX9 mutation in a previously published case of campomelic dysplasia without overt campomeliaU Friedrich, E Schaefer, P Meinecke, et al.
European Journal of Pediatrics|December 1, 1986
The velo-cardio-facial (Shprintzen) syndrome. Clinical variability in eight patientsP Meinecke, F A Beemer, A Schinzel, et al.
Clinical Genetics|February 1, 1990
Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and newbornM Ramsing, H Rehder, W Holzgreve, et al.
Journal of Clinical Pharmacy and Therapeutics|March 18, 2015
Who gets dipyrone (metamizole) in Germany? Prescribing by age, sex and regionF Hoffmann, P Meinecke, M H Freitag, et al.
American Journal of Medical Genetics|February 15, 1993
New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defectsG Gillessen-Kaesbach, P Meinecke, C Garrett, et al.
Cytogenetic and Genome Research|August 6, 2003
Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of XpK Kutsche, W Werner, O Bartsch, et al.
Calcified Tissue International|July 1, 1987
Compositional analysis of collagen from patients with diverse forms of osteogenesis imperfectaE Kirsch, T Krieg, A Nerlich, et al.
Klinische Padiatrie|March 10, 2015
Increased risk for bronchitis after discharge in non-vaccinated very low birth weight infantsG Stichtenoth, C Härtel, J Spiegler, et al.
Human Genetics|January 27, 2000
Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8H J Lüdecke, O Schmidt, J Nardmann, et al.
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