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1 t skin and mucosal erosions that typify this genodermatosis.
2 e high incidence of tumors complicating this genodermatosis.
3 r and poor prognosis of these tumors in this genodermatosis.
4 to Kindler syndrome, an autosomal-recessive genodermatosis.
5 rrelations towards understanding this severe genodermatosis.
6 for desmoplakin in the pathogenesis of this genodermatosis.
7 underlying molecular mechanisms in this rare genodermatosis.
11 chia congenita (PC) is an autosomal dominant genodermatosis caused by heterozygous mutations in any o
12 in 6 patients with Kindler syndrome (KS), a genodermatosis caused by loss of kindlin-1 (encoded by F
13 osa (RDEB), a currently incurable blistering genodermatosis caused by loss-of-function mutations in C
14 Netherton syndrome (NS) is a rare and severe genodermatosis caused by SPINK5 mutations leading to the
15 -Dube syndrome (BHD), an inherited autosomal genodermatosis characterized by benign tumors of the hai
16 Bart's syndrome was initially described as a genodermatosis characterized by congenital localized abs
17 h Neutropenia (PN) is an autosomal recessive genodermatosis characterized by early-onset poikiloderma
18 keratoderma (EPPK) is an autosomal dominant genodermatosis characterized by epidermolytic hyperkerat
19 d individuals with a new autosomal recessive genodermatosis characterized by focal and diffuse palmop
20 ogg-Dube syndrome (BHD) is a rare, inherited genodermatosis characterized by hair follicle hamartomas
21 kin syndrome (PSS) is an autosomal recessive genodermatosis characterized by lifelong, continuous she
23 Hermansky-Pudlak syndrome (HPS) is a rare genodermatosis characterized by oculocutaneous albinism,
24 todermia variabilis is an autosomal dominant genodermatosis characterized by persistent plaque-like o
25 Degos disease (DDD) is an autosomal-dominant genodermatosis characterized by reticulate pigmentation
26 s a severe, generalized, autosomal recessive genodermatosis characterized clinically by large, parchm
27 l cell carcinoma syndrome (MHIBCC) is a rare genodermatosis in which numerous indolent, well-differen
28 oric atresia (EB-PA), an autosomal recessive genodermatosis, manifests with neonatal cutaneous bliste
30 is a severe, male-lethal, X-linked, dominant genodermatosis resulting from loss-of-function mutations
31 hose of incontinentia pigmenti (IP), a human genodermatosis, synthenic with the IKK gamma/NEMO locus.
32 n-Smith Disease, is a rare cancer-associated genodermatosis with an autosomal dominant inheritance.
33 upre-Christol syndrome (BDCS)-a cancer-prone genodermatosis with an X-linked, dominant inheritance pa
34 (EKV, OMIM 133200) is an autosomal dominant genodermatosis with considerable intra- and interfamilia
35 other allele, the consequences are a severe genodermatosis with specific clinical manifestations.
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