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Metatarsal bony syndactyly in 2 fetuses with Smith-Lemli-Opitz syndrome: An under-recognized part of the clinical spectrum

Item Type:Letter
Title:Metatarsal bony syndactyly in 2 fetuses with Smith-Lemli-Opitz syndrome: An under-recognized part of the clinical spectrum
Creators Name:Moosa, S., Loeys, B., Altmüller, J., Mortier, G., Nürnberg, P., Li, Y., Wollnik, B. and Vogel, I.
Keywords:DNA Sequence Analysis, Fetus, Metatarsal Bones, Mutation, Oxidoreductases Acting on CH-CH Group Donors, Smith-Lemli-Opitz Syndrome, Syndactyly
Source:Clinical Genetics
ISSN:0009-9163
Publisher:Wiley
Volume:92
Number:3
Page Range:342-343
Date:September 2017
Official Publication:https://doi.org/10.1111/cge.12990
PubMed:View item in PubMed

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