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Results:
1-8
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Results: 8
Authors:
SCHUFFENHAUER S
LICHTNER P
PEYKARDERAKHSHANDEH P
MURKEN J
HAAS OA
BACK E
WOLFF G
ZABEL B
BARISIC I
RAUCH A
BOROCHOWITZ Z
DALLAPICCOLA B
ROSS M
MEITINGER T
Citation: S. Schuffenhauer et al., DELETION MAPPING ON CHROMOSOME 10P AND DEFINITION OF A CRITICAL REGION FOR THE 2ND DIGEORGE-SYNDROME LOCUS (DGS2), European journal of human genetics, 6(3), 1998, pp. 213-225
Authors:
LORENZ B
MIGLIACCIO C
LICHTNER P
MEYER C
STROM TM
DURSO M
BECKER J
CICCODICOLA A
MEITINGER T
Citation: B. Lorenz et al., CLONING AND GENE STRUCTURE OF THE ROD CGMP PHOSPHODIESTERASE DELTA-SUBUNIT GENE (PDED) IN MAN AND MOUSE, European journal of human genetics, 6(3), 1998, pp. 283-290
Authors:
BARTSCH O
SCHUFFENHAUER S
WAGNER A
LICHTNER P
MURKEN J
HINKEL GK
Citation: O. Bartsch et al., LOW INCIDENCE OF MICRODELETIONS AT THE 2ND DIGEORGE-SYNDROME LOCUS (10P13-14), European journal of human genetics, 6, 1998, pp. 1080-1080
Authors:
HOLZINGER A
ROSCHER AA
LANDGRAF P
LICHTNER P
KAMMERER S
Citation: A. Holzinger et al., GENOMIC ORGANIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PEROXISOMAL MEMBRANE PROTEIN-1-LIKE PROTEIN (PXMP1-L) GENE ENCODING A PEROXISOMAL ABC TRANSPORTER, FEBS letters, 426(2), 1998, pp. 238-242
SMALL PERICENTRIC-INVERSION OF CHROMOSOME-18 IN 4 UNRELATED INDIVIDUALS - A RARE CYTOGENETIC VARIANT
Authors:
SCHUFFENHAUER S
ROST I
LEDERER G
LICHTNER P
SEIDEL H
VOGTEL D
MURKEN J
Citation: S. Schuffenhauer et al., SMALL PERICENTRIC-INVERSION OF CHROMOSOME-18 IN 4 UNRELATED INDIVIDUALS - A RARE CYTOGENETIC VARIANT, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 277-277
Authors:
GOLLA A
LICHTNER P
VONGERNET S
WINTERPACHT A
FAIRLEY J
MURKEN J
SCHUFFENHAUER S
Citation: A. Golla et al., PHENOTYPIC-EXPRESSION OF THE FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 (FGFR3) MUTATION P250R IN A LARGE CRANIOSYNOSTOSIS FAMILY, Journal of Medical Genetics, 34(8), 1997, pp. 683-684
Authors:
VONGERNET S
SCHUFFENHAUER S
GOLLA A
LICHTNER P
BALG S
MUHLBAUER W
MURKEN J
FAIRLEY J
MEITINGER T
Citation: S. Vongernet et al., CRANIOSYNOSTOSIS SUGGESTIVE OF SAETHRE-CHOTZEN SYNDROME - CLINICAL DESCRIPTION OF A LARGE KINDRED AND EXCLUSION OF CANDIDATE REGIONS ON 7P, American journal of medical genetics, 63(1), 1996, pp. 177-184
Authors:
MEINDL A
CARVALHO MRS
LORENZ B
ACHATZ H
HERRMANN K
LICHTNER P
ROSS M
MEITINGER T
Citation: A. Meindl et al., CLONING OF CANDIDATE GENES FOR X-LINKED RETINITIS-PIGMENTOSA, American journal of human genetics, 57(4), 1995, pp. 1537-1537
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