MARKEDLY ELEVATED MATERNAL SERUM ALPHA-FETOPROTEIN ASSOCIATED WITH A NORMAL FETUS AND CHORIOCARCINOMA OF THE PLACENTA von Ollendorff, David A, Goldberg, Jeffrey M, Abu-Jawdeh, Graziella M, Lurain, John R

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Vaginal birth after cesarean section for arrest of labor: Is success determined by maximum cervical dilatation during the prior labor? von Ollendorff, David A., Goldberg, Jeffrey M., Minogue, John P., Socol, Michael L.

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MARKEDLY ELEVATED MATERNAL SERUM ALPHA-FETOPROTEIN ASSOCIATED WITH A NORMAL FETUS AND CHORIOCARCINOMA OF THE PLACENTA von Ollendorff, David A.

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Mélancolie de l’Europe, Stefan Zweig, Traduit par Guillaume Ollendorff et David Sanson, Présenté par Bertrand Dermoncourt , Plon, 2024, 270 p., 20 von de Lapparent, Olivier

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The value of curettage in the diagnosis of ectopic pregnancy von OLLENDORFF, D. A, FEJGIN, M. D, BARZILAI, M, BEN-NOON, I, GERBIE, A. B

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Buschke-Ollendorff syndrome: a novel case series and systematic review von Pope, V., Dupuis, L., Kannu, P., Mendoza-Londono, R., Sajic, D., So, J., Yoon, G., Lara-Corrales, I.

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Ossifying fibroma in Buschke-Ollendorff syndrome von Dawson, Annelise L., Schulman, Joshua M., Jordan, Richard C., North, Jeffrey P.

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The Buschke-Ollendorff syndrome: a case report of simultaneous osteo-cutaneous malformations in the hand von Brodbeck, Michael, Yousif, Q, Diener, P A, Zweier, M, Gruenert, J

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Deactivating Germline Mutations in LEMD3 Cause Osteopoikilosis and Buschke‐Ollendorff Syndrome, but Not Sporadic Melorheostosis von Mumm, Steven, Wenkert, Deborah, Zhang, Xiafang, McAlister, William H, Mier, Richard J, Whyte, Michael P

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Topics in Applied Mechanics. Edited by David Abir, F. Ollendorff, M. Reiner. XI + 318 S. m. Fig. u. Abb. Amsterdam/London/New York 1965. Elsevier Publishing Company. Preis geb. DM 50 von Wenzel, H.

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Buschke–Ollendorff Syndrome: Three Generations in a Japanese Family von Kawamura, Ai, Ochiai, Toyoko, Tan‐Kinoshita, Miyuki, Suzuki, Hiroyuki

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Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis von Hellemans, Jan, Debeer, Philippe, Wright, Michael, Janecke, Andreas, Kjaer, Klaus W., Verdonk, Peter C.M., Savarirayan, Ravi, Basel, Lina, Moss, Celia, Roth, Johannes, David, Albert, De Paepe, Anne, Coucke, Paul, Mortier, Geert R.

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Buschke-ollendorff syndrome: report of a case and interpretation of the clinical phenotype as a type 2 segmental manifestation of an autosomal dominant skin disease von Ehrig, Torsten, Cockerell, Clay J.

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The 12q14 microdeletion syndrome: Additional patients and further evidence that HMGA2 is an important genetic determinant for human height von Buysse, Karen, Reardon, William, Mehta, Lakshmi, Costa, Teresa, Fagerstrom, Carrie, Kingsbury, Daniel J, Anadiotis, George, McGillivray, Barbara C, Hellemans, Jan, de Leeuw, Nicole, de Vries, Bert B.A, Speleman, Frank, Menten, Björn, Mortier, Geert

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Buschke-Ollendorff syndrome of the scalp: Histologic and ultrastructural findings von Trattner, Akiva, David, Michael, Rothem, Arye, Ben-David, Eiten, Sandbank, Miriam

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Síndrome de Buschke-Ollendorff familiar von Vergara, Aránzazu, Isarría, María J., Sánchez-Caminero, Prado, Rodríguez-Peralto, José L., Guerra, Aurora

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Familial cutaneous collagenomas resulting from a novel mutation in LEMD3 von Hershkovitz, D., Amitai, D.B., Sprecher, E.

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A Model for Exploring Compatibility Between Applicants and Residency Programs: Right Resident, Right Program von Winkel, Abigail Ford, Morgan, Helen Kang, Burk-Rafel, Jesse, Dalrymple, John L., Chiang, Seine, Marzano, David, Major, Carol, Katz, Nadine T., Ollendorff, Arthur T., Hammoud, Maya M.

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A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis von Couto, Ana R, Bruges-Armas, Jacome, Peach, Chris A, Chapman, Kay, Brown, Matthew A, Wordsworth, B Paul, Zhang, Yun

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Fast and high resolution single-cell BRET imaging von Goyet, Elise, Bouquier, Nathalie, Ollendorff, Vincent, Perroy, Julie

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