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American Journal of Medical Genetics. Part A|September 5, 2003
A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHDKym M Boycott, Malcolm I Parslow, Judith L Ross, et al.
Human Brain Mapping|May 1, 2023
Adolescent brain development in girls with Turner syndromeVanessa Lozano Wun, Lara C Foland-Ross, Booil Jo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 5, 2019
Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expressionJudith L Ross, Luke Bloy, Timothy P L Roberts, et al.
The Journal of Pediatrics|April 16, 2008
Effect of ascertainment and genetic features on the phenotype of Klinefelter syndromeMartha P D Zeger, Andrew R Zinn, Najiba Lahlou, et al.
Behavioral and Brain Functions : BBF|May 23, 2007
A Turner syndrome neurocognitive phenotype maps to Xp22.3Andrew R Zinn, David Roeltgen, Gerry Stefanatos, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 17, 2020
Testicular function in boys with 47,XYY and relationship to phenotypeShanlee M Davis, Luke Bloy, Timothy P L Roberts, 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.
Pediatrics|March 14, 2012
Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndromeJudith L Ross, David P Roeltgen, Harvey Kushner, 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.
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