Meckel Gruber syndrome - a case report

Abstract Background Meckel Gruber Syndrome (MKS) is a rare autosomal recessive malformation syndrome characterized by multiple congenital anomalies ultimately leading to the death of fetus in utero or shortly after birth. It is characterized by classical triad of occipital encephalocele, infantile p...

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Main Authors: Marquess Raj (Author), Sujata Dhanuka (Author), Prerna Agarwal (Author), Suresh Lakki Reddy (Author), Sethuramalingam Vivekananthan (Author)
格式: 圖書
出版: BMC, 2020-04-01T00:00:00Z.
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索引號: A1234.567
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