Search Results - Borochowitz, Zvi U.
- Showing 1 - 7 results of 7
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SERKAL Syndrome: An Autosomal-Recessive Disorder Caused by a Loss-of-Function Mutation in WNT4 by Mandel, Hannah, Shemer, Revital, Borochowitz, Zvi U., Okopnik, Marina, Knopf, Carlos, Indelman, Margarita, Drugan, Arie, Tiosano, Dov, Gershoni-Baruch, Ruth, Choder, Mordechai, Sprecher, Eli
Published 2008Text -
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A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees by Silberstein, Mark, Weissbrod, Omer, Otten, Lars, Tzemach, Anna, Anisenia, Andrei, Shtark, Oren, Tuberg, Dvir, Galfrin, Eddie, Gannon, Irena, Shalata, Adel, Borochowitz, Zvi U., Dechter, Rina, Thompson, Elizabeth, Geiger, Dan
Published 2013Text -
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A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees by Silberstein, Mark, Weissbrod, Omer, Otten, Lars, Tzemach, Anna, Anisenia, Andrei, Shtark, Oren, Tuberg, Dvir, Galfrin, Eddie, Gannon, Irena, Shalata, Adel, Borochowitz, Zvi U., Dechter, Rina, Thompson, Elizabeth, Geiger, Dan
Published 2013Text -
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Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia by Campos-Xavier, Ana Belinda, Martinet, Danielle, Bateman, John, Belluoccio, Dan, Rowley, Lynn, Tan, Tiong Yang, Baxová, Alica, Gustavson, Karl-Henrik, Borochowitz, Zvi U., Innes, A. Micheil, Unger, Sheila, Beckmann, Jacques S., Mittaz, Lauréane, Ballhausen, Diana, Superti-Furga, Andrea, Savarirayan, Ravi, Bonafé, Luisa
Published 2009Text -
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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia by Grigelioniene, Giedre, Suzuki, Hiroshi I., Taylan, Fulya, Mirzamohammadi, Fatemeh, Borochowitz, Zvi U., Ayturk, Ugur M., Tzur, Shay, Horemuzova, Eva, Lindstrand, Anna, Weis, Mary Ann, Grigelionis, Gintautas, Hammarsjö, Anna, Marsk, Elin, Nordgren, Ann, Nordenskjöld, Magnus, Eyre, David R., Warman, Matthew L., Nishimura, Gen, Sharp, Phillip A., Kobayashi, Tatsuya
Published 2019Text -
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Morbid Obesity Resulting from Inactivation of the Ciliary Protein CEP19 in Humans and Mice by Shalata, Adel, Ramirez, Maria C., Desnick, Robert J., Priedigkeit, Nolan, Buettner, Christoph, Lindtner, Claudia, Mahroum, Mohammed, Abdul-Ghani, Muhammad, Dong, Feng, Arar, Nazik, Camacho-Vanegas, Olga, Zhang, Rui, Camacho, Sandra C., Chen, Ying, Ibdah, Mwafaq, DeFronzo, Ralph, Gillespie, Virginia, Kelley, Kevin, Dynlacht, Brian D., Kim, Sehyun, Glucksman, Marc J., Borochowitz, Zvi U., Martignetti, John A.
Published 2013Text