Myosin
发表于 2025-3-28 15:20:03
https://doi.org/10.1007/978-3-662-02409-6f intact spermatozoa with abnormal head-tail junction, and tailless heads can be present in the ejaculate (Zhu et al. 2016). This structural defect can lead to male infertility; however, successful pregnancy is possible by intracytoplasmic sperm injection (Fang et al. 2018).
PATHY
发表于 2025-3-28 20:57:42
3-Beta-Hydroxysteroid Dehydrogenase Deficiency, a 14.7 years old girl with short stature and delayed puberty; the diagnosis was made on the urinary steroid profile. It is a rare disorder described in a few families across the globe. The classic form is usually present in infancy, but cases have also been reported with onset in childhood and adults.
证实
发表于 2025-3-29 02:38:09
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goodwill
发表于 2025-3-29 05:47:24
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PAN
发表于 2025-3-29 11:15:02
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剧本
发表于 2025-3-29 14:57:23
Conclusion: Looping Back and Moving Forward,t of the enzyme and has been associated with highly variable phenotypes ranging from a neonatal form with severe neurological manifestations to an asymptomatic form that would be missed without targeted screening (Grunert et al. 2012).
Arthropathy
发表于 2025-3-29 19:12:30
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外来
发表于 2025-3-29 20:09:50
Peacekeeping: The Formative Years programs, especially in developed countries, most infants with CAH are diagnosed during the neonatal period. In the classic salt-wasting form, if not promptly identified and treated, affected infants present with a salt-wasting crisis.
exquisite
发表于 2025-3-30 00:24:38
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范例
发表于 2025-3-30 05:37:58
21 Hydroxylase Deficiency, programs, especially in developed countries, most infants with CAH are diagnosed during the neonatal period. In the classic salt-wasting form, if not promptly identified and treated, affected infants present with a salt-wasting crisis.