Disease: Hypertrichosis congenital generalized X-linked
- A new form of hypertrichosis inherited as an X-linked dominant trait
- Congenital generalized hypertrichosis terminalis: a proposed classification and a plea to avoid the ambiguous term "Ambras syndrome"
- Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
- Congenital hypertrichosis universalis in Mexican female twins
- Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait
- First Japanese case of congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Generalized hypertrichosis syndromes in Mexico
- Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1
- Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth
- Narrowing the Genomic Region of Autosomal-Dominant Congenital Generalized Hypertrichosis Terminalis
- Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis
- Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9
- X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3
- You "Cantu": Multidisciplinary Collaboration Resulting in Successful Orthognathic Surgery