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Research 271–300 of 1000+
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- The Naked (N) Mutation, Chromosome 15
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Human Trichohyalin Gene Is Clustered with the Genes for Other Epidermal Structural Proteins and Calcium-Binding Proteins at Chromosomal Locus 1q21
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- Sex-Chromosome-Related Dimorphism in Steroidogenic Enzymes and Androgen Receptor in Response to Testosterone Treatment: An In Vitro Study on Human Primary Skeletal Muscle Cells
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Sex-limited chromosomes and non-reproductive traits
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Effects of anticonvulsant drugs on chromosomes.
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation