All individuals with variants in gene CBLB

2 entries on 1 page. Showing entries 1 - 2.
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AscendingIndividual ID     

ID_report     

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VIP     

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Owner     
00019869 - PubMed: Gilissen 2014 - ? ? - - - - - - ID neonatal feeding problems and hypotonia, severe ID, macrocephaly, large cysterna magna, hydrocephalus, myelination delay and wide sulci. Seizures, self-mutilation and sleep disturbances. Facial dysmorphisms included hypertelorism, broad coarse face, low-set ears, macrostomia and mild retromicrognathia. She had small hands and feet, contractures and scoliosis. 1 1 Marianne Vos (LOVD-team)
00395614 RP-3055 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease cataract, glaucoma, rod-cone dystrophy, severe myopia, conductive hearing impairment, intellectual disability, renal atrophy, renal insufficiency 1 1 LOVD
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