Congenital abnormalities of body patterning: embryology revisited von Goodman, Frances R

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Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis von Warman, Matthew L, Gong, Yaoqin, Krakow, Deborah, Marcelino, Jose, Wilkin, Douglas, Chitayat, David, Babul-Hirji, Riyana, Hudgins, Louanne, Cremers, Cor W, Cremers, Frans P.M, Brunner, Han G, Reinker, Kent, Rimoin, David L, Cohn, Daniel H, Goodman, Frances R, Reardon, William, Patton, Michael, Francomano, Clair A

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Human HOX gene mutations von Goodman, FR, Scambler, PJ

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Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis von Superti-Furga, Andrea, Shears, Deborah J, Reardon, William, Palmer, Rodger W, Vassal, Humberto J, Scambler, Peter J, Winter, Robin M, Goodman, Frances R

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Synpolydactyly Phenotypes Correlate with Size of Expansions in HOXD13 Polyalanine Tract von Goodman, F. R., Mundlos, S., Muragaki, Y., Donnai, D., Giovannucci-Uzielli, M. L., Lapi, E., Majewski, F., McGaughran, J., McKeown, C., Reardon, W., Upton, J., Winter, R. M., Olsen, B. R., Scambler, P. J.

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Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome von Goodman, Frances R., Bacchelli, Chiara, Brady, Angela F., Brueton, Louise A., Fryns, Jean-Pierre, Mortlock, Douglas P., Innis, Jeffrey W., Holmes, Lewis B., Donnenfeld, Alan E., Feingold, Murray, Beemer, Frits A., Hennekam, Raoul C.M., Scambler, Peter J.

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Mutations in CDMP1 cause autosomal dominant brachydactyly type C von Polinkovsky, Alexander, Robin, Nathaniel H, Thomas, J. Terrig, Irons, Mira, Lynn, Audrey, Goodman, Frances R, Reardon, William, Kant, Sarina G, Brunner, Han G, van der Burgt, Ineke, Chitayat, David, McGaughran, Julie, Donnai, Dian, Luyten, Frank P, Warman, Matthew L

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A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13 von Morgan, N V, Bacchelli, C, Gissen, P, Morton, J, Ferrero, G B, Silengo, M, Labrune, P, Casteels, I, Hall, C, Cox, P, Kelly, D A, Trembath, R C, Scambler, P J, Maher, E R, Goodman, F R, Johnson, C A

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Increased nuchal translucency and split‐hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus von Bijlsma, E. K., Knegt, A. C., Bilardo, C. M., Goodman, F. R.

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Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13 von Debeer, P, Bacchelli, C, Scambler, P J, De Smet, L, Fryns, J-P, Goodman, F R

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ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome von Bacchelli, C., Wilson, L. C., Cook, J. A., Winter, R. M., Goodman, F. R.

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Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLIN von Bacchelli, C, Goodman, Fr, Scambler, Pj, Winter, Rm

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Sacral dysgenesis associated with terminal deletion of chromosome 7q : a report of two families von WANG, J, SPITZ, L, REARDON, W, HAYWARD, R, KIELY, E, HALL, C. M, O'DONOGHUE, D. P, PALMER, R, GOODMAN, F. R, SCAMBLER, P. J, WINTER, R. M

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Residential photovoltaics in the United States: status and outlook von Goodman, F.R., DeMeo, E.A., Zavadil, R.M.

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A novel acropectoral syndrome maps to chromosome 7q36 von Dundar, Munis, Gordon, Tilda M, Ozyazgan, Irfan, Oguzkaya, Fahri, Ozkul, Yusuf, Cooke, Alexander, Wilkinson, A Graham, Holloway, Susan, Goodman, Frances R, Tolmie, John L

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How often should we measure the urinary anion gap for cases of suspected renal tubular acidosis? von Streather, C P, Phillips, A O, Goodman, F R, Scoble, J E

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Childhood Traumatic Grief: An Exploration of the Construct in Children Bereaved on September 11 von Brown, Elissa J., Goodman, Robin F.

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Preaxial polydactyly in an infant with Down's syndrome von Ramanan, Av, Hussain, K, Kempley, St, Goodman, Fr

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Liposarcoma of the spermatic cord von Goodman, F R, Staunton, M D, Rees, H C

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Differential calcium movements induced by agonists in guinea pig tracheal muscle von Goodman, Frank R., Weiss, George B., Karaki, Hideaki, Nakagawa, Haruto

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