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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 18, 2024. (Total: 231582Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Turner Syndrome and SHOX[original query]
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.
The Journal of clinical endocrinology and metabolism 2002 Mar 87 (3): 1402-6.
Rappold Gudrun A, Fukami Maki, Niesler Beate, Schiller Simone, Zumkeller Walter, Bettendorf Markus, Heinrich Udo, Vlachopapadoupoulou Elpis, Reinehr Thomas, Onigata Kazumichi, Ogata Tsuto
[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study].
Orvosi hetilap 2017 8 158 (34): 1351-1356.
Dávid Anna, Butz Henriett, Halász Zita, Török Dóra, Nyir? Gábor, Muzsnai Ágota, Csákváry Violetta, Luczay Andrea, Sallai Ágnes, Hosszú Éva, Felszeghy Enik?, Tar Attila, Szántó Zsuzsanna, Fekete Gy László, Kun Imre, Patócs Attila, Bertalan Ri
Rare copy number variants in the genome of Chinese female children and adolescents with Turner syndrome.
Bioscience reports 2018 12 39 (1): .
Li Li, Li Qingfeng, Wang Qiong, Liu Li, Li Ru, Liu Huishu, He Yaojuan, Lash Gendie
Impact of parental origin of X-chromosome on clinical and biochemical profile in Turner syndrome.
Journal of pediatric endocrinology & metabolism : JPEM 2020 8 33 (9): 1155-1163.
Malhotra Rakhi, Shukla Rashmi, Kabra Madhulika, Gupta Yashdeep, Jyotsna Viveka P, Khadgawat Raje
Short stature and SHOX (Short stature homeobox) variants-efficacy of screening using various strategies.
PeerJ 2020 11 8 e10236.
Capkova Pavlina, Capkova Zuzana, Rohon Peter, Adamová Katerina, Zapletalova Jiri
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