Cold-induced sweating syndrome: CISS1 and CISS2 Manifestations from infancy to adulthood. Four new cases von HAHN, A. F, WAALER, P. E, KVISTAD, P. H, BAMFORTH, J. S, MILES, J. H, MCLEOD, J. G, KNAPPSKOG, P. M, BOMAN, H

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High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletion... von Ballif, Blake C., Rosenfeld, Jill A., Traylor, Ryan, Theisen, Aaron, Bader, Patricia I., Ladda, Roger L., Sell, Susan L., Steinraths, Michelle, Surti, Urvashi, McGuire, Marianne, Williams, Shelley, Farrell, Sandra A., Filiano, James, Schnur, Rhonda E., Coffey, Lauren B., Tervo, Raymond C., Stroud, Tracy, Marble, Michael, Netzloff, Michael, Hanson, Kristen, Aylsworth, Arthur S., Bamforth, J. S., Babu, Deepti, Niyazov, Dmitriy M., Ravnan, J. Britt, Schultz, Roger A., Lamb, Allen N., Torchia, Beth S., Bejjani, Bassem A., Shaffer, Lisa G.

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Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues von Nakabayashi, K, Makino, S, Minagawa, S, Smith, A C, Bamforth, J S, Stanier, P, Preece, M, Parker-Katiraee, L, Paton, T, Oshimura, M, Mill, P, Yoshikawa, Y, Hui, C C, Monk, D, Moore, G E, Scherer, S W

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Use of Magnetic Resonance Imaging to Measure Facial Soft Tissue Depth von Pluym, J. Vander, Shan, W. W., Taher, Z., Beaulieu, C., Plewes, C., Peterson, A. E., Beattie, O. B., Bamforth, J. S.

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X-linked situs abnormalities result from mutations in ZIC3 von Gebbia, M, Ferrero, G B, Pilia, G, Bassi, M T, Aylsworth, A, Penman-Splitt, M, Bird, L M, Bamforth, J S, Burn, J, Schlessinger, D, Nelson, D L, Casey, B

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Vitiligo-spasticity syndrome: new case von Bamforth, J S

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Congenital hypothyroidism, spiky hair, and cleft palate von Bamforth, J S, Hughes, I A, Lazarus, J H, Weaver, C M, Harper, P S

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Structural anomalies in patients with inherited metabolic diseases von Bamforth, F. J., Bamforth, J. S., Applegarth, D. A.

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Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32 von Nakabayashi, Kazuhiko, Bentley, Louise, Hitchins, Megan P., Mitsuya, Kohzoh, Meguro, Makiko, Minagawa, Sachi, Bamforth, John S., Stanier, Philip, Preece, Michael, Weksberg, Rosanna, Oshimura, Mitsuo, Moore, Gudrun E., Scherer, Stephen W.

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Homeoboxes and field defects von Bamforth, J S

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Spina bifida and hydrocephalus: a population study over a 35-year period von BAMFORTH, S. J, BAIRD, P. A

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Maternal uniparental heterodisomy for chromosome 16: Case report von Woo, V., Bridge, P. J., Bamforth, J. S.

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Congenital anomalies associated with hypothyroidism von Bamforth, J S, Hughes, I, Lazarus, J, John, R

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Are abnormalities of human organizational genes responsible for causing birth defects? von Bamforth, J.S.

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Poland anomaly with a limb body wall disruption defect: Case report and review von Bamforth, J. Stephen, Fabian, Clifford, Machin, Geoffrey, Honore, Louis

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Preservation of the morphological and molecular stability of embryonic tissues von Pinchbeck, J B, James, T L, Bagnall, K M, Bamforth, J S, Milos, N C

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Amniotic band sequence: Streeter's hypothesis reexamined von Bamforth, J. Stephen

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Technical note: Different techniques, different results—a comparison of photogrammetric and caliper‐derived measurements von Shaner, Deborah J., Bamforth, J. Stephen, Peterson, Arthur E., Beattie, Owen B.

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DK phocomelia phenotype (von Voss-Cherstvoy syndrome) caused by somatic mosaicism for del(13q) von Bamforth, J. S., Lin, C. C.

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Assessment of soft tissue facial asymmetry in medically normal and syndrome-affected individuals by analysis of landmarks and measurements von Shaner, Deborah J., Peterson, Arthur E., Beattie, Owen B., Bamforth, J. Stephen

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