APA

Jacobsen J. C., Glamuzina E., Taylor J., Swan B., Handisides S., Wilson C., Fietz M., van Dijk T., Appelhof B., Hill R., Marks R., Love D. R., Robertson S. P., Snell R. G. & Lehnert K. (20151120). Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1. : Case reports in genetics.

Chicago

Jacobsen Jessie C, Glamuzina Emma, Taylor Juliet, Swan Brendan, Handisides Shona, Wilson Callum, Fietz Michael, van Dijk Tessa, Appelhof Bart, Hill Rosamund, Marks Rosemary, Love Donald R, Robertson Stephen P, Snell Russell G and Lehnert Klaus. 20151120. Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1. : Case reports in genetics.

Harvard

Jacobsen J. C., Glamuzina E., Taylor J., Swan B., Handisides S., Wilson C., Fietz M., van Dijk T., Appelhof B., Hill R., Marks R., Love D. R., Robertson S. P., Snell R. G. and Lehnert K. (20151120). Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1. : Case reports in genetics.

MLA

Jacobsen Jessie C, Glamuzina Emma, Taylor Juliet, Swan Brendan, Handisides Shona, Wilson Callum, Fietz Michael, van Dijk Tessa, Appelhof Bart, Hill Rosamund, Marks Rosemary, Love Donald R, Robertson Stephen P, Snell Russell G and Lehnert Klaus. Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1. : Case reports in genetics. 20151120.