about
Pairomics, the omics way to mate choiceAllelic imbalance in the diagnosis of benign, atypical and malignant Spitz tumours.Laser therapy treatment of phacomatosis pigmentovascularis type II: two case reportsTrichoepithelioma papulosum multiplex.The genetics of human skin disease.Cell cycle in sporadic melanoma.Recombinogenic activity of Pantoprazole(®) in somatic cells of Drosophila melanogasterMixed vascular nevus syndrome: a report of four new cases and a literature review.Bier spots and unilateral nevoid telangiectasia: more than just a coincidenceAllelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept.Porokeratosis: present concepts.Genodermatoses caused by genetic mosaicism.Phakomatosis Pigmentovascularis Associated With Sturge-Weber Syndrome, Ota Nevus, and Congenital Glaucoma.Vascular malformation and common keratinocytic nevus of the soft type: phacomatosis pigmentovascularis revisited.Type 2 segmental trichoepitheliomatosis: a genetic concept that may explain congenital multiple trichoepitheliomas in the lines of Blaschko.Dohi Memorial Lecture. New aspects of cutaneous mosaicism.Nevoid hypertrichosis, diffuse lipoatrophy and epidermal nevus: a new syndrome?Large aberrant Mongolian spots coexisting with cutis marmorata telangiectatica congenita (phacomatosis pigmentovascularis type V or phacomatosis cesiomarmorata).Linear variant of chronic cutaneous lupus erythematosus: a clue for the pathogenesis of chronic cutaneous lupus erythematosus?Pigmentary mosaicism of the hyperpigmented type in two half-brothers.Cutaneous leiomyomatosis with type 2 segmental involvement.Assessing genotoxicity of diuron on Drosophila melanogaster by the wing-spot test and the wing imaginal disk comet assay.The categories of cutaneous mosaicism: A proposed classification.Lip cancer and pre-cancerous lesions harbor TP53 mutations, exhibit allelic loss at 9p, 9q, and 17p, but no BRAFV600E mutations.Biomarkers: paving stones on the road towards the personalized precision medicine for oral squamous cell carcinomaKlippel-Trenaunay syndromein a boy with concomitant ipsilateral overgrowth and undergrowthNevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patientsMonozygotic twin discordance for phacomatosis cesioflammea further supports the post-zygotic mutation hypothesisNevus depigmentosus and nevus of Ito: pigmentary twin spotting
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Loss of heterozygosity in human skin.
@ast
Loss of heterozygosity in human skin.
@en
type
label
Loss of heterozygosity in human skin.
@ast
Loss of heterozygosity in human skin.
@en
prefLabel
Loss of heterozygosity in human skin.
@ast
Loss of heterozygosity in human skin.
@en
P1476
Loss of heterozygosity in human skin.
@en
P2093
P304
P356
10.1016/S0190-9622(99)70042-3
P407
P433
P577
1999-08-01T00:00:00Z