Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Han-Zhi Wu"'
Publikováno v:
Reproductive and Developmental Medicine, Vol 3, Iss 2, Pp 124-127 (2019)
A 27-year-old patient with azoospermia and low intelligence was reported having a rare karyotype 47,XYY,dup(13q12.11),t(4;9)(q21.1;q22.3),r(21)(p12q22.3). Clinical genetic tests, including next-generation sequencing (NGS), karyotyping, fluorescence i
Externí odkaz:
https://doaj.org/article/01a65bec733042c586b81763f9b17bb4
Publikováno v:
Reproductive and Developmental Medicine, Vol 3, Iss 4, Pp 256-259 (2019)
A young boy with a facial abnormality was brought to our genetics clinic. Physical examination found bilateral cryptorchidism. Several clinical genetic tests, including chromosome microarray analysis (CMA), karyotyping, and azoospermia factor (AZF) m
Externí odkaz:
https://doaj.org/article/3c710b959da74239b6bd2d4284287839
Autor:
Zhan, Bin, Liu, Yan, Zhou, Wen-Ting, Li, Shu-Yi, Chen, Zhi-Biao, Stegmaier, Thomas, Aliabadi, Maryam, Han, Zhi-Wu, Ren, Lu-Quan
Publikováno v:
In Applied Surface Science 1 March 2021 541
Publikováno v:
Materials Science & Technology; Jul2024, Vol. 40 Issue 9, p665-674, 10p
Autor:
Han, Mei, Gao, Hui, Ju, Ping, Gao, Ming-quan, Yuan, Yin-ping, Chen, Xue-hong, Liu, Kai-li, Han, Yan-tao, Han, Zhi-wu
Publikováno v:
In Biomedicine & Pharmacotherapy October 2024 179
Akademický článek
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Publikováno v:
In Transactions of Nonferrous Metals Society of China 2011 21 Supplement 2:s483-s488
Publikováno v:
In Transactions of Nonferrous Metals Society of China 2011 21 Supplement 2:s380-s383
Publikováno v:
Reproductive and Developmental Medicine, Vol 3, Iss 4, Pp 256-259 (2019)
A young boy with a facial abnormality was brought to our genetics clinic. Physical examination found bilateral cryptorchidism. Several clinical genetic tests, including chromosome microarray analysis (CMA), karyotyping, and azoospermia factor (AZF) m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6470305c43f60bb50d059efa5643ff6
https://doi.org/10.4103/2096-2924.274542
https://doi.org/10.4103/2096-2924.274542
Publikováno v:
Reproductive and Developmental Medicine, Vol 3, Iss 2, Pp 124-127 (2019)
A 27-year-old patient with azoospermia and low intelligence was reported having a rare karyotype 47,XYY,dup(13q12.11),t(4;9)(q21.1;q22.3),r(21)(p12q22.3). Clinical genetic tests, including next-generation sequencing (NGS), karyotyping, fluorescence i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6198403b37cfd66b7a0540b673ba4d4e
http://www.repdevmed.org/article.asp?issn=2096-2924
http://www.repdevmed.org/article.asp?issn=2096-2924