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1
Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes.
Lin, Shan;Zeng, Jia-Bin;Zhao, Gui-Xian;Yang, Zhen-Zhen;Huang, Hui-Ping;Lin, Min-Ting;Wu, Zhi-Ying;Wa...
2019 seizure DOI: S1059-1311(19)30108-... 213 views
2
prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18
;Chih-Ping Chen;Chyi-Chyang Lin;Yi-Ning Su;Fuu-Jen Tsai;Ju-Ting Chen;Schu-Rern Chern;Chen-Chi Lee;Da...
2010 spermova DOI: 10.1016/S1028-4559(1... 238 views
3
detección de un caso de síndrome de williams-beuren por mlpa
;Sergio Laurito;Teresita Branham;Gustavo Herrero;Silvana Marsa;Fernanda Garro;María Roqué
2013 proceedings on: 2016 ieee central america and pana... 144 views

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seizure
ISSN: 1532-2688 479 views

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tsc2 genotype-phenotype correlation tsc1 tuberous sclerosis complex gynecology and obstetrics prenatal diagnosis microcephaly reciprocal translocation congenital malformations trisomy 13 trisomy 7pgynecology and obstetrics allergyinfectious and parasitic diseases