Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting Expanding the Spectrum of Autosomal Recessive ALX Related Frontonasal Dysplasia

Yerel katalogda bu makaleye atıf yapan 55 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

1. 2010 Mutation in Exon 1f of PLEC Leading to Disruption of Plectin Isoform 1f Causes Autosomal Recessive Limb Girdle Muscular DystrophyAtıf 127 · OpenAlex
2. 2010 Mutation in Exon 1f of PLEC Leading to Disruption of Plectin Isoform 1f Causes Autosomal Recessive Limb Girdle Muscular DystrophyAtıf 127 · OpenAlex
3. 2010 Mutation in Exon 1f of PLEC Leading to Disruption of Plectin Isoform 1f Causes Autosomal Recessive Limb Girdle Muscular DystrophyAtıf 126 · OpenAlex
4. 2011 Disruption of PTPRO Causes Childhood Onset Nephrotic SyndromeAtıf 118 · OpenAlex
5. 2011 Disruption of PTPRO Causes Childhood Onset Nephrotic SyndromeAtıf 118 · OpenAlex
6. 2011 Disruption of PTPRO Causes Childhood-Onset Nephrotic SyndromeAtıf 118 · OpenAlex
7. 2011 Disruption of PTPRO Causes Childhood-Onset Nephrotic SyndromeAtıf 118 · OpenAlex
8. 2011 Disruption of PTPRO Causes Childhood Onset Nephrotic SyndromeAtıf 118 · OpenAlex
9. 2011 Disruption of PTPRO Causes Childhood Onset Nephrotic SyndromeAtıf 118 · OpenAlex
10. 2011 Disruption of PTPRO Causes Childhood Onset Nephrotic SyndromeAtıf 118 · OpenAlex