All individuals with variants in gene INCENP

3 entries on 1 page. Showing entries 1 - 3.
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00207812 29122926-Fam PubMed: Ben-Salem 2018 4-generation family, 2 affected cousins, unaffected heterozygous carrier parents M yes United Arab Emirates - - - - - ? postnatal growth deficiency, profound limb shortening with proximal and distal segments involvement, narrow chest, radiological abnormalities involving spine, pelvis and metaphyses, corneal clouding and intellectual disability 1 2 Johan den Dunnen
00334635 - PubMed: Maranhao 2015 analysis 25 Pedigrees - - Pakistan - - - - - retinal disease - 1 8 LOVD
00334636 - PubMed: Maranhao 2015 analysis 25 Pedigrees - - Pakistan - - - - - retinal disease - 1 9 LOVD
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