Table 2_Prenatal diagnosis of Prader–Willi syndrome via maternal UPD15 with placental mosaicism: incidental discovery of fetal DMD carrier status.xlsx

Table 2_Prenatal diagnosis of Prader–Willi syndrome via maternal UPD15 with placental mosaicism: incidental discovery of fetal DMD carrier status.xlsx

Background<p>Prader–Willi syndrome (PWS) represents a paradigm of genomic imprinting disorders. Given the severe lifelong complications of PWS, prenatal diagnosis is crucial for early intervention and genetic counseling.</p>Methods<p>Noninvasive prenatal testing (NIPT) indicated a...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Yanchou Ye (22523684) (author)
Άλλοι συγγραφείς: Yiman Fu (22523687) (author), Zhechao Zhang (10290301) (author), Haofeng Ning (18361485) (author), Fangchao Tao (19922781) (author), Xiaonan Wang (276308) (author), Qun Fang (176267) (author), Zheng Chen (49483) (author), Xiulan Hao (12678556) (author)
Έκδοση: 2025
Θέματα:
Genetics
T15
UPD15
Prader–Willi syndrome
prenatal diagnosis
confined placental mosaicism
Duchenne muscular dystrophy
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