Zobrazeno 1 - 10
of 168
pro vyhledávání: '"G. Tariverdian"'
Autor:
G. Tariverdian, M. Paul
Das Buch ist ein Leitfaden für die tägliche Arbeit in Gynäkologie, Geburtshilfe, Neonatologie und bei der genetischen Beratung.Das Autorenteam geht auf alle sich im Rahmen der nichtinvasiven und invasiven Pränataldiagnostik stellenden Fragen ein.
Autor:
G. Tariverdian, F. Vogel
Publikováno v:
Cytogenetic and Genome Research. 91:278-284
X-linked mental retardation has recently become one of the most interesting genetic anomalies. Studying this group of conditions has led to many insights into the mechanisms involved in normal and abnormal gene actions in humans. Since the early 1980
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cefd5fed20a983b7392e0d767f98605
https://doi.org/10.1159/000056857
https://doi.org/10.1159/000056857
Autor:
P. Steinbach, D. W�hrle, G. Tariverdian, I. Kennerknecht, G. Barbi, H. Edlinger, H. Enders, M. G�tz-Sothmann, H. Heilbronner, D. Hosenfeld, R. Kircheisen, F. Majewski, P. Meinecke, E. Passarge, A. Schmidt, H. Seidel, G. Wolff, M. Zank
Publikováno v:
Human Genetics. 92:491-498
Molecular genetic analysis of the transmission of mutations in 73 families with fragile X (one of the largest samples evaluated so far) has confirmed previous hypotheses that the fragile X syndrome results from two consecutive mutational steps, desig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4250e41e4f8ca758bfa1603778aee4cb
https://doi.org/10.1007/bf00216457
https://doi.org/10.1007/bf00216457
Autor:
S, Spranger, S, Schiller, A, Jauch, K, Wolff, I, Rauterberg-Ruland, D, Hager, G, Tariverdian, J, Tröger, G, Rappold
Publikováno v:
American journal of medical genetics. 83(5)
We report on a mother and her 5-year old son, both with a terminal deletion of the short arm of the X chromosome. By molecular genetic analysis the breakpoint was located distal to steroid sulfatase gene. The boy manifested, due to nullisomy of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::25fcd45ec1dd7bf4f75b4ab86d4a495b
https://pubmed.ncbi.nlm.nih.gov/10232745
https://pubmed.ncbi.nlm.nih.gov/10232745
Publikováno v:
American journal of medical genetics. 82(5)
Oculo-facio-cardio-dental syndrome is a very rare condition. So far, only nine cases have been documented. We report on three additional female patients representing the same entity. The clinical findings were: congenital cataract, microphthalmia/mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c31069ff167761b7429c1d3736e6046
https://pubmed.ncbi.nlm.nih.gov/10069716
https://pubmed.ncbi.nlm.nih.gov/10069716
Autor:
C, Sergi, B R, Schulze, H D, Hager, B, Beedgen, E, Zilow, O, Linderkamp, H F, Otto, G, Tariverdian
Publikováno v:
Pathologica. 90(3)
A female fetus showing severe growth retardation was delivered at 31 weeks of gestation because of fetal distress. At birth, the infant showed bradycardia and no spontaneous breathing. Although high frequency oscillatory ventilation was started, seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::48b1b1a0f20de4a2cb56bb6854a50432
https://pubmed.ncbi.nlm.nih.gov/9774859
https://pubmed.ncbi.nlm.nih.gov/9774859
Publikováno v:
European journal of pediatrics. 155(9)
We report on a 13-month old boy with microcephalic osteodysplastic primordial dwarfism (MOPD), whose radiographic signs correspond with type II of this entity. Some of his clinical signs, such as the anomalies of the external genitalia and the urinar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a11dd4ab7e05c45cbd337557d0d6adc
https://pubmed.ncbi.nlm.nih.gov/8874115
https://pubmed.ncbi.nlm.nih.gov/8874115
Autor:
E. Glauner, C. Baldermann, A. Bardhan, Susumu Ohno, A. Mannan, C. Althaus, R. Brauner, E. Schnakenberg, K. Hirschhorn, W. Krone, G. Williams, B.H.F. Weber, K. Sperling, G.A. Rappold, K.R. Held, J.S. Schinfeld, J. Seidel, H. Guedes-Pinto, H. Berninger, O.J. Miller, M. Kämper, M.J. Wakefield, H.L. Schulz, W.K. Holloman, M. Schmidt, M. Krawczak, B. Petersen, S. Kußmann, N. Mah, S. Fröhlich, M. Fellous, Helmut Baitsch, M.L. Houck, T. Bonk, D. Bächner, B. Skawran, L.G. Kömüves, J. Andrich, W. Vogel, T.O. Goecke, Y.-F.C. Lau, P.M. Chou, U. Zechner, N.B. Atkin, V. Beensen, D.K. Lamatsch, andK. Benirschke, H.P. Klinger, A. Rosenthal, T. Dörk, A. Gal, R. Melcher, G. Tariverdian, S. Ebner, P.E. Warburton, W. Schloot, P. Miny, C. Kelbova, J. Neesen, C. Reuter, M.S. Magid, K. Lücke, U. Drews, M. Rosemblatt, W. Jaggernauth, S. Knauf, E. Günther, A. Rump, C. Backsch, B. Gharavi, K. Trenz, M. Stumm, M. Wilda, V. Kalscheuer, S. Stengel-Rutkowski, B. Schröder, R. von Golitschek, H. Bostelmann, J. Schmidtke, U. Klein-Vogler, D. Schlote, J.T. Epplen, L. Walter, T. Grimm, S.S. Wachtel, S.C. Kingswood, M.P. Achary, F. Jaubert, H. Przuntek, C. Steinlein, U. Langenbeck, M. Schöning, W. Kress, H. Enders, A. Schinzel, S. Kümmerle, R. Breuer, B. Levy, I. Nanda, C. Nihoul-Feketé, S. Henschel, K. Schiebel, H. Kehrer-Sawatzki, H.G. Nothwang, H. Stöhr, M. Winkelmann, C. Groß, C.R. Mueller, W. Schempp, P. Kaiser, C. Saft, S.G. Somkuti, N.A. Ellis, M. Gencik, F. Vogel, R. Chaves, P. Schütz, P.R. Papenhausen, H. Neitzel, M. Schartl, R. Werdin, A.P. Singh, A. Epplen, G. Senger, J.H. Tepperberg, L. Setterfield, M.M. Sanz, K. Dreikorn, F. Dechend, A.J. Kersten, T. Liehr, M. Schmid, H. Hameister, A. Alfieri, C. Tyler-Smith, A.T. Kumamoto, S.J. Charter, S. Schubert, C. Dixkens, M. Büsse, S. Balg, U. Grumpelt, L. Salas-Cortés, H. Collmann, B. Vikram, K. Fredga, H.M. Schüler, P. Wieacker, A. Humeny, E. Passarge, M.B. Petersen, K. Kainer, G. Herzberger, J. Meder, S. Röttger, H. Hoehn, S. Jakubiczka, T.M. Dunn, B. Halliger-Keller, W. Mosgoeller, R. Bendix, J.S. Heslop-Harrison, S.K. Bohlander, E.P. Evans, E.M. Bühler, I. Hansmann, R. Toder, M. Mikkelsen, K. Kutsche, D. Schindler, P. Burfeind, T. Haaf, J. Frowein, H.G. Schwarzacher, M. Döbler-Neumann, T. Sharma, B. Eiben, P.H. Yen, N.B. Kardon, J. German, M. Proytcheva, H. Winking, G. Speit, G. Scherer, C. Fischer, K. Eggermann, A. Pomarino, A. Hehr, A. Dufke, E. Reichl, W. Engel, S. Avenarius, P.S. Burgoyne, J.A. Alonzo, T. Schwarzacher, A. Gehrig, T.O. Schulz, J.A.M. Graves, E. Gross, U. Müller, J.C. Iezzoni, U. Mittwoch, S. Fallet, J.J. Pasantes
Publikováno v:
Cytogenetic and Genome Research. 91:310-311
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::865bd151f37551cde267ef49a2033538
https://doi.org/10.1159/000056865
https://doi.org/10.1159/000056865
Autor:
H. Kehrer-Sawatzki, G. Williams, H. Berninger, O.J. Miller, K. Dreikorn, F. Dechend, M. Kämper, T. Bonk, V. Beensen, N. Mah, S. Balg, S. Jakubiczka, W. Schloot, I. Hansmann, M. Wilda, D. Schindler, K. Lücke, A. Hehr, G. Herzberger, T. Liehr, H.G. Nothwang, A. Bardhan, S. Henschel, A. Dufke, N.A. Ellis, J.S. Heslop-Harrison, S.K. Bohlander, K. Eggermann, M. Gencik, T.M. Dunn, R. Werdin, L. Setterfield, L. Walter, W. Vogel, M.P. Achary, K. Kainer, M. Schmid, S. Kußmann, R. Bendix, C. Nihoul-Feketé, K. Schiebel, W. Engel, S. Avenarius, B. Gharavi, E. Passarge, G. Tariverdian, H.L. Schulz, K. Trenz, D.K. Lamatsch, J. Frowein, P. Schütz, H. Neitzel, M.S. Magid, C. Steinlein, T. Grimm, J. Meder, T. Dörk, M. Fellous, M. Stumm, G. Senger, J.A. Alonzo, M.B. Petersen, H. Enders, M.L. Houck, S. Kümmerle, U. Grumpelt, R. Chaves, W. Mosgoeller, P.E. Warburton, A.T. Kumamoto, B. Schröder, R. Melcher, P.H. Yen, K. Kutsche, J.T. Epplen, C. Kelbova, H.G. Schwarzacher, D. Schlote, M. Döbler-Neumann, P.M. Chou, R. Brauner, F. Jaubert, J. Neesen, M. Proytcheva, B. Eiben, J. German, C. Reuter, J.J. Pasantes, G. Scherer, H. Winking, Y.-F.C. Lau, U. Zechner, V. Kalscheuer, Susumu Ohno, M. Winkelmann, A. Mannan, W. Jaggernauth, E. Reichl, P.S. Burgoyne, E. Glauner, S. Knauf, H. Przuntek, S.G. Somkuti, U. Müller, C. Baldermann, andK. Benirschke, C. Backsch, A. Gehrig, H. Stöhr, H.P. Klinger, M.M. Sanz, S. Fröhlich, M.J. Wakefield, T.O. Goecke, J.C. Iezzoni, C. Dixkens, M. Büsse, C. Althaus, R. Breuer, B. Levy, I. Nanda, A. Epplen, B. Vikram, E. Schnakenberg, P. Miny, R. Toder, L. Salas-Cortés, C. Groß, F. Vogel, P.R. Papenhausen, E.M. Bühler, A. Rump, U. Langenbeck, M. Schöning, W.K. Holloman, M. Schmidt, A. Alfieri, H. Collmann, S.C. Kingswood, K.R. Held, Helmut Baitsch, P. Burfeind, T. Haaf, J.A.M. Graves, E. Gross, S. Ebner, B.H.F. Weber, T. Sharma, K. Sperling, U. Klein-Vogler, J. Seidel, H. Guedes-Pinto, G. Speit, B. Petersen, J. Schmidtke, K. Hirschhorn, A.P. Singh, M. Krawczak, L.G. Kömüves, B. Halliger-Keller, M. Mikkelsen, N.B. Kardon, C. Fischer, W. Krone, J.S. Schinfeld, A. Schinzel, M. Rosemblatt, S.S. Wachtel, W. Kress, A.J. Kersten, C.R. Mueller, C. Saft, W. Schempp, A. Humeny, J.H. Tepperberg, N.B. Atkin, S. Schubert, H.M. Schüler, P. Wieacker, G.A. Rappold, R. von Golitschek, H. Bostelmann, J. Andrich, S. Röttger, P. Kaiser, M. Schartl, H. Hameister, C. Tyler-Smith, S.J. Charter, K. Fredga, E.P. Evans, H. Hoehn, D. Bächner, B. Skawran, U. Mittwoch, A. Rosenthal, A. Gal, S. Fallet, U. Drews, A. Pomarino, E. Günther, T. Schwarzacher, T.O. Schulz, S. Stengel-Rutkowski
Publikováno v:
Cytogenetic and Genome Research. 91:308-309
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89974e94ddc464ffe59edfbe3dc465f0
https://doi.org/10.1159/000056864
https://doi.org/10.1159/000056864
Autor:
J, Klapp, K H, Nicolaides, H D, Hager, T, Voigtländer, J, Greiner, G, Tariverdian, W D, Lehmann
Publikováno v:
Geburtshilfe und Frauenheilkunde. 50(6)
Preliminary clinical experience with early amniocentesis is reported. Fifty-two amniocenteses were performed before the end of the 14th week following the last menstrual period. Cytogenetic and biochemical analyses (AFP, AChE) were performed. Increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c672e8523d02de2907e45c866c3b7c8
https://pubmed.ncbi.nlm.nih.gov/1695882
https://pubmed.ncbi.nlm.nih.gov/1695882