A family at risk of congenital adrenal hyperplasia: A molecular approach for prenatal diagnosis
The molecular method for prenatal diagnosis in the first trimester was carried out on the second and third pregnancies of a family at risk of congenital adrenal hyperplasia (CAH). The first child, an 8-year-old daughter, was affected. The molecular and cytogenetic prenatal diagnosis on the second pr...
Saved in:
Main Authors: | Pornpimol Ruangvutilert, Kitirat Techatraisak, Sujin Kanokpongsakdi |
---|---|
Other Authors: | Mahidol University |
Format: | Article |
Published: |
2018
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/26652 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
Similar Items
-
Congenital adrenal hyperplasia
by: Loke, K.Y.
Published: (2013) -
Clinical applications of molecular genetics: the model of congenital adrenal hyperplasia.
by: Loke, K.Y.
Published: (2011) -
Clinical applications of molecular genetics: The model of congenital adrenal hyperplasia
by: Loke, K.Y.
Published: (2016) -
Case Report: Diagnosis and Management of Adrenal Crisis in 46XX Congenital Adrenal Hyperplasia Infant
by: Nur Rochmah, -, et al.
Published: (2022) -
Case Report: Diagnosis and Management of Adrenal Crisis in 46XX Congenital Adrenal Hyperplasia Infant
by: Nur Rochmah, -, et al.
Published: (2022)