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American Journal of Human Genetics|September 14, 2000
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.American Journal of Medical Genetics|September 6, 1996
Isochromosome Xq in Klinefelter syndrome: report of 7 new casesS Arps, T Koske-Westphal, P Meinecke, et al.Klinische Padiatrie|January 20, 2010
Surfactant without intubation in preterm infants with respiratory distress: first multi-center dataAngela Kribs, C Härtel, E Kattner, et al.American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.Nature Genetics|June 3, 2000
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determinationK W Gripp, D Wotton, M C Edwards, et al.Neonatology|July 3, 2009
Polymorphisms in the Renin-Angiotensin system and outcome of very-low-birthweight infantsJ Spiegler, A Gilhaus, I R Konig, et al.Klinische Padiatrie|March 24, 2012
Major contributors to hospital mortality in very-low-birth-weight infants: data of the birth year 2010 cohort of the German Neonatal NetworkG Stichtenoth, M Demmert, B Bohnhorst, et al.Nature Genetics|December 30, 1999
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type IP Momeni, G Glöckner, O Schmidt, et al.American Journal of Medical Genetics|March 13, 1995
Further delineation of the branchio-oculo-facial syndromeA E Lin, R J Gorlin, I W Lurie, et al.American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.Pageof 8