All individuals with variants in gene MAD2L2

2 entries on 1 page. Showing entries 1 - 2.
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00081424 - PubMed: Bluteau 2016, Journal: Bluteau 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents F - France - - - - - FANC severe bone marrow failure (HP:0005528) involving all 3 lineages (hemoglobin, 8.0 g/dl; neutrophil count, 0.43×10ˆ9/l; platelets, 10 × 10^9/l), Fanconi anemia physical signs (short size (HP:0004322) at less than tenth percentile, microcephaly (HP:0000252), abnormal facial features (HP:0000271)), renal tubulopathy (HP:0000091), elevated serum alpha-fetoprotein (HP:0006254), positive mitomycine C (MMC) chromosome breakage test blood lymphocytes 1 1 Johan den Dunnen
00390029 16 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Very pale optic disk, chorioretinal atrophy in macular area, highly altered fundus 1 1 LOVD
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