Search Results - Kalff-Suske, Martha

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  1. 1
    Subcutaneous progesterone versus vaginal progesterone for luteal phase support in in vitro fertilization: A retrospective analysis from daily clinical practice

    Subcutaneous progesterone versus vaginal progesterone for luteal phase support in in vitro fertilization: A retrospective analysis from daily clinical practice by Schütt, Marcel, Nguyen, The Duy, Kalff-Suske, Martha, Wagner, Uwe, Macharey, Georg, Ziller, Volker

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  2. 2
    All Human Genes of the Uteroglobin Family Are Localized on Chromosome 11q12.2 and Form a Dense Cluster

    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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  3. 3
    Molecular Characterization of Human Zyxin

    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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  4. 4
    Subcutaneous progesterone versus vaginal progesterone for luteal phase support in in vitro fertilization: A retrospective analysis from daily clinical practice

    Subcutaneous progesterone versus vaginal progesterone for luteal phase support in in vitro fertilization: A retrospective analysis from daily clinical practice by Schutt, Marcel, Nguyen, The Duy, Kalff-Suske, Martha, Wagner, Uwe, Macharey, Georg, Ziller, Volker

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  5. 5
    Point Mutations in Human GLI3 Cause Greig Syndrome

    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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  6. 6
    Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome

    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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  7. 7
    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

    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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  8. 8
    The human S3a ribosomal protein: sequence, location and cell-free transcription of the functional gene

    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.

    Published in Gene
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  9. 9
    Human Sp3 Transcriptional Regulator Gene (SP3) Maps to Chromosome 2q31

    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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  10. 10
    Human Sp4 transcription factor gene (SP4) maps to chromosome 7p15

    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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