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Research 91–120 of 1000+
- Retorno de la fertilidad en un perro con un abscesso prostático
- Woolly hair generalizado: caso clínico e revisão da literatura
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- Claves diagnósticas en displasias pilosas II
- Anomalous Fluorescence of White Hair Compared to Other Unpigmented Keratin Fibres
- The eyelash follicle features and anomalies: A review
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Hair Anomalies in a 6-Year-Old Girl
- The trichoscopic features of hair shaft anomalies induced by epidermal growth factor receptor inhibitors: A case series
- Nutrition and Hair Anomalies
- Avaliação de alterações estruturais envolvendo o surgimento de tecido adiposo em localizações anômalas e o deslocamento de glândulas crinas em três alopecias cicatriciais primárias linfocíticas
- Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.
- Ulerythema ophryogenes with multiple congenital anomalies
- Management of Adult Facial Vascular Anomalies
- Bubble hair and other acquired hair shaft anomalies due to hot ironing on wet hair
- Recurrent Pregnancy Loss Associated Cytogenetic and Genetic Anomalies – Study from Eastern India
- No Relationship Between Perceived Health Anomalies and Perceived Experimental Success in Retired Breeder Male Hartley Albino Guinea Pigs
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Guadalupe fur seal alopecia: a metabolic syndrome associated to climatic anomalies?
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Familial Background in Aberrant Mammary Tissue Is a ‘Protective’ Factor against the Development of Nephrourinary Anomalies
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- 860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Hormonal Organization of Sex Differences in Play Fighting and Spatial Behavior
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Exposure to gamma-rays at the telogen phase of the hair cycle inhibits hair follicle regeneration at the anagen phase in mice