Zobrazeno 1 - 10
of 236
pro vyhledávání: '"G, Tariverdian"'
Autor:
Walter, H.
Publikováno v:
Anthropologischer Anzeiger, 2000 Mar 01. 58(1), 123-124.
Externí odkaz:
https://www.jstor.org/stable/29540926
Autor:
Bullerdiek, J.
Publikováno v:
Anthropologischer Anzeiger, 1997 Dec 01. 55(3/4), 381-381.
Externí odkaz:
https://www.jstor.org/stable/29540743
Autor:
Bullerdiek, J.
Publikováno v:
Anthropologischer Anzeiger, 1996 Mar 01. 54(1), 89-90.
Externí odkaz:
https://www.jstor.org/stable/29540583
Autor:
M. Keil
Publikováno v:
Biologie in unserer Zeit. 22:131-132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffb5b5dff76b73387f3ad6bd0cd2f854
https://doi.org/10.1002/biuz.19920220311
https://doi.org/10.1002/biuz.19920220311
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