All individuals with variants in gene TBL1XR1

6 entries on 1 page. Showing entries 1 - 6.
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00050457 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? long nose, thick upper lip vermilion, upslanted palpebral fissure, large fleshy ears, wide intermamillary distance, brachydactyly syndrome, global developmental delay 1 1 Johan den Dunnen
00050571 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, hemangioma, oral cleft, seizures, abnormality of the skeletal system, optic disc pallor 1 1 Johan den Dunnen
00207894 28771251-Pat107 PubMed: Lionel 2018 - F - Canada - - - - - ? Global developmental delay; seizures; generalized hypotonia 1 1 Johan den Dunnen
00416253 Pat10 PubMed: Monroe 2016 - M - Netherlands - - - - - ? 36w-birth with an omphalocele, Apgar score of 2/7, development delayed from birth; cyclic neutropenia, trombopathy caused by storage pool deficiency; diminished fasting tolerance resulting in hypoglycemia, disturbed gastric tract motility, nephropcalcinosis, delayed myelinization; muscle biopsy revealed diminished ATP production, diminished activity of multiple complexes, no mitochondrial DNA abnormalities 1 1 Johan den Dunnen
00440412 PED2185.1 PubMed: Nambot 2018 - - - France - - - - - ? - 1 1 Johan den Dunnen
00458107 - - - M - - (not applicable) white - - - - NDD HP:0001263, HP:0000750, HP:0000271, HP:0000708 1 1 Marketa Wayhelova
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