14q12 Microdeletion syndrome and congenital variant of Rett syndrome.doi: 10.1016/j.ejmg.2009.03.004. [ Cross Ref ]Mencarelli MA,
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interstitial deletion 16(q12. 1q13) of paternal origin in a 10-year-old boydoi:10.1111/j.1399-0004.1992.tb03249.x
HIGH DENSITY EXPANSION OF THE CRITICAL TEMPERATURE By solving recursively the (1413)9=780−310142/03qq163 + 13104q12 − + 41895984q5 60104q11 +
u00dcber eine ungewu00f6hnliche Schu00e4digung der Grou03b2hirnrinde durch Insulindoi:10.1159/000148532European Neurology
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(e.g. normal body temperature or absence of (high producer) was reduced in pts P=0.03 12 12q12 VDR GD exon 2 initiation codon (VDR
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(first yellow highlight) sequence in the hominid37313894 17q12-q21 6 chr9:133458833 9q34.2 703 28 2615 1.53E-03 28 2621 1.59E-03 2
(-1) or high level gains (+1) indicating 0.03 0.90 ± 0.09 9.67 ± 2.44 Gender 5q12.3-q13.1 RP11-475K24 RP11-417A16 65.9
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of which two novel nonsense mutations Q2X and Q123X, resulted in doi:10.1016/S0960-9822(03)00067-8Komatireddy SChakrabarti S
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Highlight Terms Gene Ontology(2) Diseases(2) D11S1917*03-H0570POLYA*02, which was under-locus on chromosome 11q12–13 in type 1
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