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Research 181–210 of 1000+
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Bloom's syndrome–‐a first report from India
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Chapter 6. Darwinian Health and Other Contradictions
- (673) Seminoma in SRY-Negative 46, XX Testicular Disorder of Sex Development Presenting as Acute Abdomen: An Extremely Rare Case Report
- 651 Epigenetic regulation of macrophage activity by glutamine during wound healing
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- BIPHENOTYPIC LEUKAEMIA
- Allelic frequencies for the seventeen Y-STR loci observed in Iraqi male patients with prostate cancer
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- 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
- 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
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- The Sex-Linked Histocompatibility Antigens
- 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
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia
- Down Syndrome and Autoimmune Disease
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic