An optimized set of human telomere clones for studying telomere integrity and architecture
Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S, Regan R, Brenan M, Nicod A, Lawrie NM, Cardy DL, Nguyen H, Hudson TJ, Riethman HC, Ledbetter DH, Flint J. An optimized set of human telomere clones for studying telomere integrity and architecture. Am J Hum Genet 2000; 67: 320-332.
Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal
Fryns JP, Kleczkowska A, Casaer P, van den Berge H. Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal. Ann Genet 1986; 29: 49-52.
Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses
Vialard F, Ottolenghi C, Gonzales M, Choiset A, Girard S, Siffroi JP, McElreavey K, Vibert-Guigue C, Sebaoun M, Joye N, Portnoi MF, Jaubert F, Fellous M. Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses. J Med Genet 2002; 39: 514-518.
Impaired male sex development in an infant with molecularly defined partial 9p monosomy: Implication for a testis forming gene(s) on 9p
Ogata T, Muroya K, Matsuo N, Hata J, Fukushima YSY. Impaired male sex development in an infant with molecularly defined partial 9p monosomy: Implication for a testis forming gene(s) on 9p. J Med Genet 1997; 34: 331-334.