Point Mutations in Human GLI3 Cause Greig Syndrome by Wild, Anja, Kalff-Suske, Martha, Vortkamp, Andrea, Bornholdt, Dorothea, Kônig, Rainer, Grzeschik, Karl-Heinz

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Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations by Debeer, Philippe, Peeters, H., Driess, S., De Smet, L., Freese, K., Matthijs, G., Bornholdt, D., Devriendt, K., Grzeschik, K.-H., Fryns, J.-P., Kalff-Suske, M.

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Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome by Kalff-Suske, Martha, Wild, Anja, Topp, Juliane, Wessling, Martina, Jacobsen, Eva-Maria, Bornholdt, Dorothea, Engel, Hartmut, Heuer, Heike, Aalfs, Cora M., Ausems, Margreet G. E. M., Barone, Rita, Herzog, Andreas, Heutink, Peter, Homfray, Tessa, Gillessen-Kaesbach, Gabriele, König, Rainer, Kunze, Jürgen, Meinecke, Peter, Müller, Dietmar, Rizzo, Renata, Strenge, Sibylle, Superti-Furga, Andrea, Grzeschik, Karl-Heinz

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Gene symbol: GLI3. Disease: Pallister-Hall syndrome by Kalff-Suske, M, Paparidis, Z, Bornholdt, D, Cole, T, Kalff-Suske, M, Grzeschik, K-H

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Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality by Williams, Patricia Gail, Hersh, Joseph H., Yen, Frank F., Barch, Margaret J., Kleinert, Harold E., Kunz, J., Kalff‐Suske, M.

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All Human Genes of the Uteroglobin Family Are Localized on Chromosome 11q12.2 and Form a Dense Cluster by NI, JIAN, KALFF-SUSKE, MARTHA, GENTZ, REINER, SCHAGEMAN, JEOFFREY, BEATO, MIGUEL, KLUG, JÖRG

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Molecular Characterization of Human Zyxin by Macalma, Teresita, Otte, Jürgen, Hensler, Mary E., Bockholt, Susanne M., Louis, Heather A., Kalff-Suske, Martha, Grzeschik, Karl-Heinz, von der Ahe, Dietmar, Beckerle, Mary C.

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Effects of opening the incubator on morphokinetics in mouse embryos by Nguyen, TNQ, Sommer, S, Greene, B, Wrenzycki, C, Kalff-Suske, M, Wagner, U, Ziller, V

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Influence of different oxygen concentrations on mouse embryo development using time-lapse-imaging by Nguyen, TNQ, Bardua, I, Greene, B, Wrenzycki, C, Kalff-Suske, M, Wagner, U, Ziller, V

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Human Sp4 transcription factor gene (SP4) maps to chromosome 7p15 by Kalff-Suske, Martha, Kunz, Jürgen, Grzeschik, Karl-Heinz, Suske, Guntram

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Lutealphasensubstitution in der ART – vaginale Progesteronsubstitution versus subkutane Applikation in der täglich klinischen Anwendung by Schuett, M, Greene, B, Kalff-Suske, M, Wagner, U, Ziller, V

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The human S3a ribosomal protein: sequence, location and cell-free transcription of the functional gene by Nolte, Dagmar, Taimor, Gerhild, Kalff-Suske, Martha, Seifart, Klaus H.

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Human Sp3 Transcriptional Regulator Gene (SP3) Maps to Chromosome 2q31 by Kalff-Suske, Martha, Kunz, Jürgen, Grzeschik, Karl-Heinz, Suske, Guntram

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Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: Not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individual by Sobetzko, Diana, Eich, Georg, Kalff-Suske, Martha, Grzeschik, Karl-Heinz, Superti-Furga, Andrea

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Gene symbol: GLI3. Disease: Pallister-Hall syndrome by Freese, K, Driess, S, Bornholdt, D, Shoenle, E J, Seidel, H, Tinschert, S, Grzeschik, K-H, Kalff-Suske, M

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Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndrome by Driess, S, Freese, K, Bornholdt, D, Kobelt, A, Kress, W, Mortier, G, Radhakrishna, U, Antonarakis, S E, Rauch, A, Suri, M, Verheij, J B G M, Woerle, H, Grzeschik, K-H, Kalff-Suske, M

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Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality by Williams, Patricia Gail, Hersh, Joseph H., Yen, Frank F., Barch, Margaret J., Kleinert, Harold E., Kunz, J., Kalff-Suske, M.

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