Cite
HARVARD Citation
Basit, S. et al. (2018). Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2. Congenital anomalies. pp. 56-61. [Online].
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Basit, S. et al. (2018). Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2. Congenital anomalies. pp. 56-61. [Online].