Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions von Tan, Tiong Yang, Gonzaga-Jauregui, Claudia, Bhoj, Elizabeth J., Strauss, Kevin A., Brigatti, Karlla, Puffenberger, Erik, Li, Dong, Xie, LiQin, Das, Nanditha, Skubas, Ioanna, Deckelbaum, Ron A., Hughes, Virginia, Brydges, Susannah, Hatsell, Sarah, Siao, Chia-Jen, Dominguez, Melissa G., Economides, Aris, Overton, John D., Mayne, Valerie, Simm, Peter J., Jones, Bryn O., Eggers, Stefanie, Le Guyader, Gwenaël, Pelluard, Fanny, Haack, Tobias B., Sturm, Marc, Riess, Angelika, Waldmueller, Stephan, Hofbeck, Michael, Steindl, Katharina, Joset, Pascal, Rauch, Anita, Hakonarson, Hakon, Baker, Naomi L., Farlie, Peter G.

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Co-option of the cardiac transcription factor Nkx2.5 during development of the emu wing von Farlie, Peter G., Davidson, Nadia M., Baker, Naomi L., Raabus, Mai, Roeszler, Kelly N., Hirst, Claire, Major, Andrew, Mariette, Mylene M., Lambert, David M., Oshlack, Alicia, Smith, Craig A.

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Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology von Farlie, Peter G., Baker, Naomi L., Yap, Patrick, Tan, Tiong Y.

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Ruthenium cryptates with an unusual selectivity for nitrate von Baker, Naomi C A, Fletcher, Nicholas C, Horton, Peter N, Hursthouse, Michael B

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'This sad time': The Augustinian Temporality of 'King Lear' von Baker, Naomi

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Attitudes toward long-acting reversible contraception among young women seeking abortion von Rose, Sally B, Cooper, Annette J, Baker, Naomi K, Lawton, Beverley

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New insights into dihydrogenphosphate recognition with dirhenium( i ) tricarbonyl complexes bridged by a thiourea moiety von Blackburn, Anna L., Baker, Naomi C. A., Fletcher, Nicholas C.

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Secretion and Assembly of Type IV and VI Collagens Depend on Glycosylation of Hydroxylysines von Sipilä, Laura, Ruotsalainen, Heli, Sormunen, Raija, Baker, Naomi L., Lamandé, Shireen R., Vapola, Miia, Wang, Chunguang, Sado, Yoshikazu, Aszodi, Attila, Myllylä, Raili

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Reduction of Lysyl Hydroxylase 3 Causes Deleterious Changes in the Deposition and Organization of Extracellular Matrix von Risteli, Maija, Ruotsalainen, Heli, Salo, Antti M., Sormunen, Raija, Sipilä, Laura, Baker, Naomi L., Lamandé, Shireen R., Vimpari-Kauppinen, Leena, Myllylä, Raili

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Application of Genome Sequencing from Blood to Diagnose Mitochondrial Diseases von Rius, Rocio, Compton, Alison G., Baker, Naomi L., Welch, AnneMarie E., Coman, David, Kava, Maina P., Minoche, Andre E., Cowley, Mark J., Thorburn, David R., Christodoulou, John

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Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy von Baker, Naomi L., Mörgelin, Matthias, Peat, Rachel, Goemans, Nathalie, North, Kathryn N., Bateman, John F., Lamandé, Shireen R.

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Clinical and Molecular Characterisation of Children with Pierre Robin Sequence and Additional Anomalies von Xu, Jessie X., Kilpatrick, Nicky, Baker, Naomi L., Penington, Anthony, Farlie, Peter G., Tan, Tiong Yang

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Molecular consequences of dominant Bethlem myopathy collagen VI mutations von Baker, Naomi L., Mörgelin, Matthias, Pace, Rishika A., Peat, Rachel A., Adams, Naomi E., Gardner, R. J. McKinlay, Rowland, Lewis P., Miller, Geoffrey, De Jonghe, Peter, Ceulemans, Berten, Hannibal, Mark C., Edwards, Matthew, Thompson, Elizabeth M., Jacobson, Richard, Quinlivan, Ros C. M., Aftimos, Salim, Kornberg, Andrew J., North, Kathryn N., Bateman, John F., Lamandé, Shireen R.

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Collagen VI glycine mutations: Perturbed assembly and a spectrum of clinical severity von Pace, Rishika A., Peat, Rachel A., Baker, Naomi L., Zamurs, Laura, Mörgelin, Matthias, Irving, Melita, Adams, Naomi E., Bateman, John F., Mowat, David, Smith, Nicholas J. C., Lamont, Phillipa J., Moore, Steven A., Mathews, Katherine D., North, Kathryn N., Lamandé, Shireen R.

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Olfr603, an orphan olfactory receptor, is expressed in multiple specific embryonic tissues von Baker, Naomi L., Miller, Kerry A., Newgreen, Donald F., Farlie, Peter G.

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Collagen VI Microfibril Formation Is Abolished by an α2(VI) von Willebrand Factor Type A Domain Mutation in a Patient with Ullrich Congenital Muscular Dystrophy von Tooley, Leona D., Zamurs, Laura K., Beecher, Nicola, Baker, Naomi L., Peat, Rachel A., Adams, Naomi E., Bateman, John F., North, Kathryn N., Baldock, Clair, Lamandé, Shireen R.

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The comparison of fac and mer ruthenium(ii) trischelate complexes in anion binding von Baker, Naomi C A, McGaughey, Neil, Fletcher, Nicholas C, Chernikov, Aleksey V, Horton, Peter N, Hursthouse, Michael B

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Effects of Early Atipamezole Reversal of Medetomidine-Ketamine Anesthesia in Mice von Baker, Naomi J, Schofield, John C, Caswell, Mark D, McLellan, Alexander D

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SORE DISTRACTION: HAMLET, AUGUSTINE AND TIME von Baker, Naomi

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‘Sore distraction’: Hamlet, Augustine and Time von Baker, Naomi

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