M. Tadin-Strapps

Genetic Hair and Nail Defects

A. Christiano, M. Tadin-Strapps, 2006 .

Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome

T. Gilliam, A. Christiano, D. Warburton, 2004, Cytogenetic and Genome Research.

A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis.

A. Christiano, A. Martinez-Mir, H. Lam, 2004, The Journal of investigative dermatology.

Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X‐linked trait

A. Christiano, A. Martinez-Mir, A. Christiano, 2003, Clinical genetics.

Fishing for new genes in skin biology: impact of cytogenetics on gene discovery

A. Christiano, D. Warburton, M. Tadin-Strapps, 2004, Clinical genetics.

Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis

V. Jobanputra, Yufeng Shen, Yujun Han, 2013, Proceedings of the National Academy of Sciences of the United States of America.

Identification of mutations in the COL7A1 gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency

D. Bickers, A. Martinez-Mir, L. Horev, 2003, Clinical and experimental dermatology.

A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.

J. Sundberg, A. Christiano, D. Warburton, 2008, Human molecular genetics.

Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth

V. Jobanputra, A. Christiano, B. Levy, 2014, PLoS genetics.