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Items: 2

1.
Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth
Bhavi P. Modi, Hardik I. Parikh, Maria E. Teves, Rewa Kulkarni, Jiang Liyu, Roberto Romero, Timothy P. York, Jerome F. Strauss, III
BMC Med Genet. 2018; 19: 181. Published online 2018 Oct 5. doi: 10.1186/s12881-018-0696-4
PMCID:
PMC6173941
AbstractArticlePDF–383K
2.
Unique autosomal recessive variant of palmoplantar keratoderma associated with hearing loss not caused by known mutations
Moustafa Abdelaal Hegazi, Sommen Manou, Hazem Sakr, Guy Van Camp
An Bras Dermatol. 2017 Sep-Oct; 92(5 Suppl 1): 154–158. doi: 10.1590/abd1806-4841.20176235
PMCID:
PMC5726709
AbstractArticlePDF–283K

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