Construction of a Detailed Physical and Transcript Map of the Candidate Region for Russell–Silver Syndrome on Chromosome 17q23–q24 von Dörr, Sylvia, Midro, Alina T., Färber, Claudia, Giannakudis, Joannis, Hansmann, Ingo

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Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature von Dutta, Usha R, Hansmann, Ingo, Schlote, Dietmar

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20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits von Lalani, S R, Thakuria, J V, Cox, G F, Wang, X, Bi, W, Bray, M S, Shaw, C, Cheung, S W, Chinault, A C, Boggs, B A, Ou, Z, Brundage, E K, Lupski, J R, Gentile, J, Waisbren, S, Pursley, A, Ma, L, Khajavi, M, Zapata, G, Friedman, R, Kim, J J, Towbin, J A, Stankiewicz, P, Schnittger, S, Hansmann, I, Ai, T, Sood, S, Wehrens, X H, Martin, J F, Belmont, J W, Potocki, L

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Cystatin C (CST3), the Candidate Gene for Hereditary Cystatin C Amyloid Angiopathy (HCCAA), and Other Members of the Cystatin Gene Family Are Clustered on Chromosome 20p11.2 von Schnittger, Susanne, Rao, V.V.N.Gopal, Abrahamson, Magnus, Hansmann, Ingo

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Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome von Röpke, Albrecht, Kujat, Annegret, Gräber, Mechthild, Giannakudis, Joannis, Hansmann, Ingo

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Paramutation-Like Effects at the Mouse scapinin (Phactr3) Locus von Worch, Sebastian, Hansmann, Ingo, Schlote, Dietmar

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Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements von Starke, Heike, Seidel, Jörg, Henn, Wolfram, Reichardt, Sylvia, Volleth, Marianne, Stumm, Markus, Behrend, Christine, Sandig, Klaus R, Kelbova, Christine, Senger, Gabriele, Albrecht, Beate, Hansmann, Ingo, Heller, Anita, Claussen, Uwe, Liehr, Thomas

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Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome von Fischer, Andreas, Klamt, Barbara, Schumacher, Nina, Glaeser, Christiane, Hansmann, Ingo, Fenge, Hartmut, Gessler, Manfred

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Association of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritis von Dörr, Sylvia, Lechtenböhmer, Nadine, Rau, Rolf, Herborn, Gertraud, Wagner, Ulf, Müller-Myhsok, Bertram, Hansmann, Ingo, Keyszer, Gernot

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Pattern and frequency of nondisjunction in oocytes from the Djungarian hamster are determined by the stage of first meiotic spindle inhibition von HUMMLER, E, HANSMANN, I

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An excess of chromosome 1 breakpoints in male infertility von BACHE, Ihen, VAN ASSCHE, Elvire, KALSCHEUER, Vera, LIEBAERS, Inge, BONDUELLE, Maryse, TOURNAYE, Herman, AYUSO, Carmen, BARBI, Gotthold, BLENNOW, Elisabeth, BOURROUILLOU, Georges, BRONDUM-NIELSEN, Karen, BRUUN-PETERSEN, Gert, CINGOZ, Sultan, CROQUETTE, Marie-Francoise, DAHOUN, Sophie, DALLAPICCOLA, Bruno, DAVISON, Val, DELOBEL, Bruno, DUBA, Hans-Christoph, DUPREZ, Laurence, FERGUSON-SMITH, Malcolm, FITZPATRICK, David R, GRACE, Elizabeth, BUGGE, Merete, HANSMANN, Ingo, HULTEN, Maj, JENSEN, Peter Ka, JONVEAUX, Philippe, KRISTOFFERSSON, Ulf, LOPEZ-PAJARES, Isidora, MCGOWAN-JORDAN, Jean, MURKEN, Jan, ORERA, Maria, PARKIN, Tony, TÜMER, Zeynep, PASSARGE, Eberhard, RAMOS, Carmen, RASMUSSEN, Kirsten, SCHEMPP, Werner, SCHUBERT, Regine, SCHWINGER, Eberhard, SHABTAI, Fiorella, SMITH, Kim, STALLINGS, Raymond, STEFANOVA, Margarita, HJORTH, Mads, TRANEBJERG, Lisbeth, TURLEAU, Catherine, BIRGER VAN DER HAGEN, Carl, VEKEMANS, Michel, KOKALJ VOKAC, Nadja, WAGNER, Klaus, WAHLSTROEM, Jan, ZELANTE, Leopoldo, TOMMERUP, Niels, LUNDSTEEN, Claes, LESPINASSE, James, WINTHER, Kirsten, NIEBUHR, Anita

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Twelve novel JAG1 gene mutations in polish Alagille syndrome patients von Jurkiewicz, Dorota, Popowska, Ewa, Gläser, Christiane, Hansmann, Ingo, Krajewska-Walasek, Małgorzata

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Duplication of Xq26.2-q27.1, including SOX3, in a mother and daughter with short stature and dyslalia von Stankiewicz, Paweł, Thiele, Hannelore, Schlicker, Mike, Cseke-Friedrich, Andrea, Bartel-Friedrich, Sylva, Yatsenko, Svetlana A., Lupski, James R., Hansmann, Ingo

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Gene symbol: JAG1. Disease: tetralogy of Fallot von Glaeser, C, Kotzot, Dieter, Caliebe, Almuth, Kottke, Renate, Schulz, Susanne, Schweigmann, Ullrich, Hansmann, Ingo

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Molecular Structure and Chromosomal Mapping of the Human Homolog of the Agouti Gene von Kwon, Heajoon Y., Bultman, Scott J., Löffler, Christiane, Chen, Wen-Ji, Furdon, Paul J., Powell, John G., Usala, Anton-Lewis, Wilkison, William, Hansmann, Ingo, Woychik, Richard P.

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Twelve novel JAG1 gene mutations in polish Alagille syndrome patients: MUTATIONS IN BRIEF von Jurkiewicz, Dorota, Popowska, Ewa, Gläser, Christiane, Hansmann, Ingo, Krajewska-Walasek, Małgorzata

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Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage von EIBEN, B, BARTELS, I, RAUSKOLB, R, HANSMANN, I, BAÊHR-PORSCH, S, BORGMANN, S, GATZ, G, GELLERT, G, GOEBEL, R, HAMMANS, W, HENTEMANN, M, OSMERS, R

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Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome: MUTATIONS IN BRIEF von Röpke, Albrecht, Kujat, Annegret, Gräber, Mechthild, Giannakudis, Joannis, Hansmann, Ingo

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Genomic structure of karyopherin α2 (KPNA2) within a low-copy repeat on chromosome 17q23-q24 and mutation analysis in patients with Russell-Silver syndrome von DÖRR, Sylvia, SCHLICKER, Mike, HANSMANN, Ingo

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Parental mosaicism of JAG1 mutations in families with Alagille syndrome von Giannakudis, J, Röpke, A, Kujat, A, Krajewska-Walasek, M, Hughes, H, Fryns, J P, Bankier, A, Amor, D, Schlicker, M, Hansmann, I

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