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The New England Journal of Medicine|April 1, 2011
Growth hormone plus childhood low-dose estrogen in Turner's syndromeJudith L Ross, Charmian A Quigley, Dachuang Cao, et al.
Hormones and Behavior|October 7, 2014
Brain responses to sexual images in 46,XY women with complete androgen insensitivity syndrome are female-typicalStephan Hamann, Jennifer Stevens, Janice Hassett Vick, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2008
Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450sccChan Jong Kim, Lin Lin, Ningwu Huang, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 14, 2025
Growth and Growth-Promoting Treatments in Turner SyndromeRoopa Kanakatti Shankar, Charmian A Quigley, Tsuyoshi Isojima, et al.
Hormone Research in Paediatrics|April 29, 2010
Growth hormone treatment does not affect incidences of middle ear disease or hearing loss in infants and toddlers with Turner syndromeMarsha L Davenport, Jackson Roush, Chunhua Liu, et al.
The Journal of Clinical Endocrinology and Metabolism|October 19, 2006
Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency: Two-year results of a randomized, controlled, multicenter trialWerner F Blum, Brenda J Crowe, Charmian A Quigley, et al.
Hormone Research|February 4, 2009
Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndromeWerner F Blum, Dachuang Cao, Volker Hesse, et al.
Journal of Medical Genetics|December 22, 2006
Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiencyGudrun Rappold, Werner F Blum, Elena P Shavrikova, et al.
Hormone Research in Paediatrics|April 11, 2019
Genetic Polymorphisms Associated with Idiopathic Short Stature and First-Year Response to Growth Hormone TreatmentCharmian A Quigley, Ying Grace Li, Milton R Brown, et al.
The Journal of Pediatrics|October 18, 2005
The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndromeJudith L Ross, Karen Kowal, Charmian A Quigley, et al.
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