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1 ructural and regulatory proteins--also cause Seckel syndrome.
2 lead to the neurodevelopmental disorder, ATR-Seckel syndrome.
5 elangiectasia mutated and Rad3 related (ATR)-Seckel syndrome and autosomal recessive primary microcep
6 ders of extreme growth failure (for example, Seckel syndrome and Majewski osteodysplastic primordial
7 NT) gene were identified in individuals with Seckel syndrome and microcephalic osteodysplastic primor
10 A damage-response pathway, is mutated in ATR-Seckel syndrome (ATR-SS), a disorder characterized by se
11 taxia telangiectasia and RAD3-related) cause Seckel syndrome (ATR-SS), a microcephalic primordial dwa
16 ve been reported in primary microcephaly and Seckel syndrome, disorders without the hallmark clinical
17 more, we find that cells of individuals with Seckel syndrome due to mutations in PCNT (PCNT-Seckel) h
20 ct identified in the developmental disorder, Seckel syndrome, is a mutation in ataxia telangiectasia
21 xtreme global growth failure (which includes Seckel syndrome, microcephalic osteodysplastic primordia
25 nts with defective ATR signalling, including Seckel syndrome, Nijmegen breakage syndrome and MCPH-1-d
32 centrosomal protein whose gene is mutated in Seckel syndrome (SCKL, MIM 210600), an inherited recessi
34 ich is mutated in the microcephalic disorder Seckel syndrome, sustains cerebellar growth by maintaini
35 We previously mapped a locus associated with Seckel syndrome to chromosome 3q22.1-q24 in two consangu
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