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Research 421–450 of 1000+
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- 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
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- 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>
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- 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
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia
- The Sex-Linked Histocompatibility Antigens
- Down Syndrome and Autoimmune Disease
- Eruptive syringomas in Down’s syndrome
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- PERBANDINGAN ARMS-PCR DAN ALLELE-SPECIFIC PCR DALAM OPTIMASI GENOTIPING SNP rs1998076
- Sex Reversal in Birds
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>