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Research 601–630 of 1000+
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Central centrifugal cicatricial alopecia: possible familial aetiology in two African families from South Africa
- Familial Sexual Precocity
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Familial frontal fibrosing alopecia in two male families
- Familial hypertriglyceridemia in pregnancy
- Familial Androgenetic Alopecia in Siblings with Normal Endocrinological Status
- Familial patterns of alopecia areata: A systematic review and meta-analysis
- Familial Background in Aberrant Mammary Tissue Is a ‘Protective’ Factor against the Development of Nephrourinary Anomalies
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Familial congenital generalized hypertrichosis
- Familial coexistence of vitiligo and alopecia areata: successful treatment with intralesional corticosteroids
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- How safe and effective is minoxidil for familial baldness in women?
- Familial association of polycystic ovary syndrome (PCOS) in women attending the gynaecological endocrinology clinic at Groote Schuur Hospital
- Analysis of familial history in Chinese patients with androgenetic alopecia
- New familial association between ocular coloboma and loose anagen syndrome
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Acne neonatorum and Familial Hyperandrogenism
- Cantú syndrome with coexisting familial pituitary adenoma
- A new familial presentation of dissecting cellulitis: The genetic implications on scarring alopecias
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Vitiligo – Study In view of familial occurence
- BIOCHEMICAL FACTORS INFLUENCING FAMILIAL HIRSUTISM IN THE SOUTHERN REGION OF KPK
- Identification of Familial Infections Using Multilocus Microsatellite Typing in Tinea Corporis due to <i>Microsporum canis</i>
- Cutaneous xanthomas in homozygous familial hypercholesterolemia: A 12-year follow-up