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  • 1-10 of  54 results for ""Congenital Malformation""
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Academic Journal

Recurrent human 16p11.2 microdeletions in type I Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome patients in Chinese Han population.

  • Source: Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-10. 10p.

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Academic Journal

A novel variant of GLI3, p.Asp1514Thrfs*5, is identified in a Chinese family affected by polydactyly.

  • Source: Molecular Genetics & Genomic Medicine. Jul2022, Vol. 10 Issue 7, p1-8. 8p.

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Academic Journal

Epidemiological statistics of congenital thumb duplication in the Chinese population.

  • Source: Journal of Orthopaedic Surgery & Research. 8/9/2021, Vol. 16 Issue 1, p1-5. 5p.

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  • 1-10 of  54 results for ""Congenital Malformation""