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	46,XY complete gonadal dysgenesis in a familial case with a rare mutation in the Desert Hedgehog (DHH) gene
	Neocleous, Vassos 1,2; Fanis, Pavlos 1,2; Cinarli, Feride 1,2; Oulas, Anastasios 2,3; Spyrou, George M.2,3; Phylactou, Leonidas A.1,2; Skordis, Nicos 1,4,5
来源期刊	HORMONE RESEARCH IN PAEDIATRICS
ISSN	1663-2818
EISSN	1663-2826
出版年	2019
卷号	91 页码:489-489
类型	Meeting Abstract
语种	英语
国家	Cyprus
收录类别	SCI-E
WOS记录号	WOS:000485922404249
WOS类目	Endocrinology & Metabolism ; Pediatrics
WOS研究方向	Endocrinology & Metabolism ; Pediatrics
资源类型	期刊论文
条目标识符	http://119.78.100.177/qdio/handle/2XILL650/216139
作者单位	1.Cyprus Inst Neurol & Genet, Dept Mol Genet Funct & Therapy, Nicosia, Cyprus; 2.Cyprus Sch Mol Med, Nicosia, Cyprus; 3.Cyprus Inst Neurol & Genet, Bioinformat Grp, Nicosia, Cyprus; 4.Paedi Ctr Specialized Pediat, Div Pediat Endocrinol, Nicosia, Cyprus; 5.Univ Nicosia, St Georges Univ London, Med Sch, Nicosia, Cyprus
推荐引用方式 GB/T 7714	Neocleous, Vassos,Fanis, Pavlos,Cinarli, Feride,et al. 46,XY complete gonadal dysgenesis in a familial case with a rare mutation in the Desert Hedgehog (DHH) gene[J],2019,91:489-489.
APA	Neocleous, Vassos.,Fanis, Pavlos.,Cinarli, Feride.,Oulas, Anastasios.,Spyrou, George M..,...&Skordis, Nicos.(2019).46,XY complete gonadal dysgenesis in a familial case with a rare mutation in the Desert Hedgehog (DHH) gene.HORMONE RESEARCH IN PAEDIATRICS,91,489-489.
MLA	Neocleous, Vassos,et al."46,XY complete gonadal dysgenesis in a familial case with a rare mutation in the Desert Hedgehog (DHH) gene".HORMONE RESEARCH IN PAEDIATRICS 91(2019):489-489.