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Keyword [TCOF1]
Result: 1 - 4 | Page: 1 of 1
1. Family Collection, Phenotype Analysis And Genetic Study Of Goldenhar Syndrome
2. Neural Tube Defects Affected Subject Carrying Rare Variant TCOF1 Gene A491g Disrupts Ribosome Biosynthesis
3. Phenotype Analysis And Genetic Study Of Chinese Treacher Collins Syndrome Patients
4. Bioinformatics Analysis Of The Genetics Of Microtia Syndrome
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