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Research 61–90 of 160
- National scientific medical meeting 1996 abstracts
- Cutaneous manifestations of systemic infection in children
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Evaluation of anti-Zika virus activities of broad-spectrum antivirals and NIH clinical collection compounds using a cell-based, high-throughput screen assay
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Trichothiodystrophy in a child with occult learning disorder
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Biotin Supplementation Ameliorates Murine Colitis by Preventing NF-κB Activation
- Genetic hair and nail disorders
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Primary Essential Cutis Verticis Gyrata: A Case Report with a Review of Literature
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Low Heterozygosity and Historical Bottleneck Effect Depicted From the Genome Assembly of the Indus River Dolphin (<i>Platanista minor</i>)
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Plasma Diaphanous Related Formin 1 Levels Are Associated with Altered Glucose Metabolism and Insulin Resistance in Patients with Polycystic Ovary Syndrome: A Case Control Study
- Lysophospholipid Mediators in Health and Disease
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Frequency of neuro-psychiatric dysfunction in anti-SSA/SSB exposed children with and without neonatal lupus
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies