EP05.11: Prenatal diagnosis of Beare‐Stevenson cutis gyrata syndrome von Park, J.

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Tracheal cartilaginous sleeve in patients with Beare‐Stevenson syndrome von Seki, Eijun, Enomoto, Keisuke, Tanoue, Koji, Tanaka, Mio, Kurosawa, Kenji

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Report of a Father With Congenital Bilateral Absence of the Vas Deferens Fathering a Child With Beare-Stevenson Syndrome von Ferreira, Leonardo C, Dantas Junior, José H

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p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice von Wang, Yingli, Zhou, Xueyan, Oberoi, Kurun, Phelps, Robert, Couwenhoven, Ross, Sun, Miao, Rezza, Amélie, Holmes, Greg, Percival, Christopher J, Friedenthal, Jenna, Krejci, Pavel, Richtsmeier, Joan T, Huso, David L, Rendl, Michael, Jabs, Ethylin Wang

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Beare-Stevenson syndrome: Two new patients, including a novel finding of tracheal cartilaginous sleeve von Wenger, Tara L., Bhoj, Elizabeth J., Wetmore, Ralph F., Mennuti, Michael T., Bartlett, Scott P., Mollen, Thomas J., McDonald-McGinn, Donna M., Zackai, Elaine H.

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Chronotopes of exile and loss in Philip O'Sullivan Beare's Zoilomastix (c. 1626) von Tracey, Kevin Gerard

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The 2022 Hedley Beare oration: Surf's up: Reflections on the current era of educational reform von Sandra Milligan

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Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome von Slavotinek, Anne, Crawford, Howard, Golabi, Mahin, Tao, Cathy, Perry, Hazel, Oberoi, Sneha, Vargervik, Karin, Friez, Michael

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Reply to Beare von Lockington, D

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‘To Beare the Towne Harmles’: Manorial Regulation of Mobility and Settlement in Early Modern Lancashire von WATSON, CHRIS

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A Case of Beare-Stevenson Syndrome with Unusual Manifestations von Ron, Nitin, Leung, Samuel, Carney, Erin, Gerber, Alexis, David, Karen Laurie

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The effect of a Beare‐Stevenson syndrome Fgfr2 Y394C mutation on early craniofacial bone volume and relative bone mineral density in mice von Percival, Christopher J., Wang, Yingli, Zhou, Xueyan, Jabs, Ethylin W., Richtsmeier, Joan T.

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Beare-Stevenson Syndrome: Two Dutch Patients With Cerebral Abnormalities von Barge-Schaapveld, Daniela Q.C.M., MD, PhD, Brooks, Alice S., MD, PhD, Lequin, Maarten H., MD, PhD, van Spaendonk, Rosalinda, Vermeulen, R. Jeroen, MD, PhD, Cobben, Jan Maarten, MD, PhD

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Licking the 'beare whelpe': William Lambarde and Matthew Parker Revise the Perambulation of Kent von McMahon, Madeline

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p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice von Wang, Yingli, Zhou, Xueyan, Oberoi, Kurun, Phelps, Robert, Couwenhoven, Ross, Sun, Miao, Rezza, Amelie, Holmes, Greg, Percival, Christopher J, Friedenthal, Jenna, Krejci, Pavel, Richtsmeier, Joan T, Huso, David L, Rendl, Michael, Jabs, Ethylin Wang

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Beare-Stevenson syndrome: Rare case report von Kariyappa, Mallesh, Sekhon, Prabjyoth, Javarappa, Prakash, Shilpa, S

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Fibroblast growth factor receptor 2 mutations in Beare–Stevenson cutis gyrata syndrome von Przylepa, Kelly A., Paznekas, William, Zhang, Minghuang, Golabi, Mahin, Bias, Wilma, Bamshad, Michael J., Carey, John C., Hall, Bryan D., Stevenson, Roger, Orlow, Seth J., Cohen Jr, M. Michael, Jabs, Ethylin Wang

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In memoriam: Margaret Evelyn BEARE (1946–2019) von Stevanović, Aleksandar

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Second case of Beare–Stevenson syndrome with an FGFR2 Ser372Cys mutation von Fonseca, Renata, Costa‐Lima, Marcelo A., Cosentino, Viviana, Orioli, Iêda M.

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AB037. The first case of Beare-Stevenson cutis gyrata syndrome with an FGFR2 gene mutation (Tyr375Cys) in Thailand von Wichajarn, Khunton, Kiatchoosakul, Pakaphan, Komwilaisak, Ratana

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