All individuals with variants in gene HPRT1

9 entries on 1 page. Showing entries 1 - 9.
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00000086 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 2 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 3 1 Yu Sun
00050635 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, joint hypermobility, sparse scalp hair, sparse lateral eyebrow, highly arched eyebrow, strabismus, edema, spontaneous neonatal pneumothorax, umbilical hernia, hypopigmentation of the skin, 3-4 toe syndactyly, sandal gap, ventriculomegaly, generalized neonatal hypotonia, nocturnal hypoventilation, hip dysplasia, unilateral ptosis, upslanted palpebral fissure, inverted nipples 1 1 Johan den Dunnen
00294941 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00374345 S-2482 PubMed: Ganapathy 2019 - - - India - - - - - ? Features suggestive of dystonia 1 1 Johan den Dunnen
00414705 NA01899 PubMed: Bell 2011 - ? - - - - - - - retinal disease - 1 1 LOVD
00427955 Pat8 PubMed: Boone 2010 2-generation family, 1 affected, unaffected carrier mother M - United States - - - - - LNS see paper; ..., mild developmental delay, failure to thrive 1 1 Johan den Dunnen
00467689 - - - F - Germany - - - - - HPRT-related gout - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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