All individuals with variants in gene TRPS1

18 entries on 1 page. Showing entries 1 - 18.
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00081135 - - - - - Germany - - - - - TRPS1 - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00100191 - PubMed: Sun 2016 3-generation family, affected proband, father and uncle M - (China) - - - - - BD - 1 3 Arrate Pereda
00103753 No 1 PubMed: Momeni 2000 2 generation family, two affected (mother and son) M ? (Germany) - - - - - TRPS1 brachydactyly; delayed bone maturation; no calcification; no intellectual disability; postnatal growth retardation; stature, short, mild (HPO_0003502) 1 2 Arrate Pereda
00103770 No 2 PubMed: Momeni 2000 - F - (Germany) - - - - - TRPS1 - 1 4 Arrate Pereda
00103771 No 3 PubMed: Momeni 2000 - M - (Germany) - - - - - TRPS1 - 1 4 Arrate Pereda
00103775 No 4 PubMed: Momeni 2000 - ? - (Germany) - - - - - TRPS1 - 1 1 Arrate Pereda
00103776 No 5 PubMed: Momeni 2000 - F - (Germany) - - - - - TRPS1 - 1 1 Arrate Pereda
00103803 No 6 PubMed: Momeni 2000 - M - (Germany) - - - - - TRPS1 - 1 1 Arrate Pereda
00116803 - - - - - Germany - - - - - TRPS1 - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00121860 - - - F yes Lebanon Lebanon - - - - CHD - 1 4 Georges Nemer
00133222 - - - - - - - - - - - TRPS1 - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00134069 - NOT PUBLISHED - F no China - - - - - TRPS1 cone-shaped epiphysis middle phalanges; ulnar and radius epiphysis hypoplasia; flattened femoral epiphysis; sparse scalp hair; bulbous nose; brachydactyly-E; no delayed bone maturation; no calcification; dysmorphic face; short stature (<3rd centile) 1 1 Arrate Pereda
00265864 - - - - - - - - - - - TRPS1 - 1 1 Margot Cousin
00265884 - - - - - - - - - - - TRPS1 - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00288330 - - - - - - - - - - - TRPS1 - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00397619 Tab4-Pat12 PubMed: Zhang 2015 - - - China - - - - - dysplasia, bone see paper; ... 1 1 Johan den Dunnen
00462227 - - - F - - - - - - - TRPS1 - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00469827 - PubMed: Jacob 2025 2-generation family, 1 affected, unaffected non-carrier parents - - India - - - - - skeletal dysplasia - 1 1 Johan den Dunnen
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