1. Abe K, Matsuda I, Matsuura N, Murayama T, Uzuki K, Endo M, Miyakoshi M, Okuno A (1976) X-linked ichthyosis, bilateral cryptorchidism, hypogenitalism and mental retardation in two siblings. Clin Genet 9: 341345
2. Aldridge J, Kunkel L, Bruns G, Tantravahi U, Lalande M, Brester T, Moreau E, Wilson M, Bromley W, Roderick T, Latt SA (1984) A strategy to reveal high-frequency RFLPs along the human X chromosome. Am J Hum Genet 36: 546–564
3. Baehner RL, Kunkel LM, Monaco AP, Haines JL, Conneally PM, Palmer C, Heerema N, Orkin SH (1986) DNA linkage analysis of X chromosome-linked chronic granulomatous disease. Proc Natl Acad Sci USA 83: 3398–3401
4. Ballabio A, Parenti G, Tippett P, Mondello C, Di Maio S, Tenore A, Andria G (1985) X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome. Hum Genet 72: 237–240
5. Barakat AY, Papadopoulou ZL, Chandra RS, Hollerman CE, Calcagno PL (1974) Pseudohermaphroditism, nephron disorder and Wilms’ tumor: a unifying concept. Pediatrics 54: 366–369