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Research 181–210 of 1000+
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Allelic frequencies for the seventeen Y-STR loci observed in Iraqi male patients with prostate cancer
- BIPHENOTYPIC LEUKAEMIA
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Genetic mechanism of androgenic alopecia
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- XX/XY chimerism in tortoiseshell tomcats – a new case and review of the literature
- Ponatinib-induced pityriasis rubra pilaris-like adnexal dysmaturation: A case report
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- Down Syndrome and Autoimmune Disease
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia
- The Sex-Linked Histocompatibility Antigens
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Secondary Cicatricial and other Permanent Alopecias
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Molecular basis of androgen insensitivity
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.