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Showing results (31-40 of 33) with videos related to

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Neurogenetics|May 28, 2009
SCA27 caused by a chromosome translocation: further delineation of the phenotypeD Misceo, M Fannemel, T Barøy, et al.
Human Genetics|November 3, 1998
Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndromeT Tvrdik, S Marcus, S M Hou, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
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Showing results (31-40 of 33) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 33 results.
Neurogenetics|May 28, 2009
SCA27 caused by a chromosome translocation: further delineation of the phenotypeD Misceo, M Fannemel, T Barøy, et al.
Human Genetics|November 3, 1998
Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndromeT Tvrdik, S Marcus, S M Hou, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
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