| 1 | LPHAS, WNT7A
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| Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation.
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| Kantaputra PN, Kapoor S, Verma P, Kaewgahya M, Kawasaki K, Ohazama A, Ketudat Cairns JR.
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| Eur J Med Genet 60(12):695-700. doi: 10.1016/j.ejmg.2017.09.005. Epub 2017 Sep 14.
2017
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| 2 | LPHAS, WNT7A
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| A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus.
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| Mutlu MB, Cetinkaya A, Koc N, Ceylaner G, Erguner B, Aydın H, Karaman S, Demirci O, Goksu K, Karaman A.
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| Eur J Med Genet 59(11):604-606. doi: 10.1016/j.ejmg.2016.09.009. Epub 2016 Sep 13.
2016
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| 3 | WNT7A, LPHAS
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| Al-Awadi/Raas-Rothschild syndrome: two new cases and review.
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| Lonardo F, Sabba G, Luquetti DV, Monica MD, Scarano G.
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| Am J Med Genet A 143(24):3169-74. 2007
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| 4 | LPHAS, WNT7A
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| Mutations in WNT7A cause a range of limb malformations, including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.
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| Woods CG, Stricker S, Seemann P, Stern R, Cox J, Sherridan E, Roberts E, Springell K, Scott S, Karbani G, Sharif SM, Toomes C, Bond J, Kumar D, Al-Gazali L, Mundlos S.
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| Am J Hum Genet 79(2):402-8. Epub 2006 Jun 23. 2006
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