Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome
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Marni J. Falk | Nathan R. Wilson | E. Zackai | H. Hakonarson | R. Chiavacci | J. Allanson | I. Saadi | P. Kruszka | M. Muenke | M. Deardorff | M. Harr | M. Falk | D. McDonald-McGinn | D. Swarr | John P. Johnson | Dong Li | Cindy Hudson | E. McCormick | R. Hart | Ariel F. Martinez | Mindy H Li