Kidney agenesis in 2 generations. on the problem of humane genetic counseling in Potter syndrome
Anger, H.; Weber, G.; Witkowski, R.
Padiatrie und Grenzgebiete 23(4): 189-193
1984
ISSN/ISBN: 0030-932X PMID: 6483447 Document Number: 241651
Document emailed within 1 workday
Related Documents
Rodríguez-García, R. 1999: Bilateral renal agenesis (Potter's syndrome) in a girl born to a hyperthyroid mother who received methimazole in early pregnancy Ginecologia y Obstetricia de Mexico 67: 587-589Sherman, S.L. 1991: Genetic epidemiology of the fragile X syndrome with special reference to genetic counseling Progress in Clinical and Biological Research 368: 79-99
Steffelaar, J.W.; van Collenburg, J.J.; Niermeyer, M.F. 1980: Polycystic kidney disorders, genetic counseling and prenatal diagnosis Nederlands Tijdschrift Voor Geneeskunde 124(49): 2073-2079
Ramaswami, P.K.; Senior, D.C. 1979: Klinefelter's syndrome with agenesis of kidney, diabetes, hyperlipoproteinaemia and stroke British Journal of Clinical Practice 33(5): 142-143
Christodorescu, D. 1980: Genetic counseling for neurological and psychic diseases 1. data on counselees and their pre counseling and post counseling family planning Revue Roumaine de Medecine Neurologie et Psychiatrie 18(4): 269-280
Rott, H.D. 1973: Genetic counseling in Down's syndrome Zeitschrift für Allgemeinmedizin 49(29): 1405-1407
Pierson, M.; Faulon, M.; Vigneron, J.; Leheup, B. 1985: Genetic counseling and the caudal regression syndrome Journal de Genetique Humaine 33(5): 405-418
Eibach, U.; Eibach-Bialas, A. 1981: Genetic counseling, prenatal diagnosis and ethics. Position in the publication of the Scientific Committee of German Physicians "Genetic Counseling and prenatal diagnosis in West Germany" Die Medizinische Welt 32(39): 1453-1455
Liubchenko, L.N. 2011: Li-Fraumeni syndrome: clinico-molecular diagnostics and medico-genetic counseling Vestnik Rossiiskoi Akademii Meditsinskikh Nauk 12: 47-52
Hauser, G.; Maier, U.; Mohl, W. 1984: Dermatoglyphics in families with Potter type IIi polycystic kidney degeneration Wiener Klinische Wochenschrift 96(21): 801-804
Tamayo, M.L.; Lopez, G.; Gelvez, N.; Medina, D.; Kimberling, W.J.; Rodríguez, V.; Tamayo, G.E.; Bernal, J.E. 2008: Genetic counseling in Usher syndrome: linkage and mutational analysis of 10 Colombian families Genetic Counseling 19(1): 15-27
Kristoffersson, U.; Wahlström, J.; Lynöe, N. 2005: New discoveries about the fragile X syndrome complicate genetic counseling. More symptoms than earlier known caused by the disease gene Lakartidningen 102(44): 3232-4 3236
Iglesias, J.; Pardo, H.; Klein, F.; Leyton, M.; Capetillo, M. 1981: Potter syndrome Revista Chilena de Obstetricia y Ginecologia 46(4): 220-227
Halmai, M.; Kosztolányi, G. 1985: Value of genetic counseling in the light of the outcome of pregnancies following counseling Orvosi Hetilap 126(14): 845-848
Carrasco Alonso, M.; Aitken Lavanchy, S.; Atala Yazigi, C. 1988: Potter's syndrome: a clinical case Revista Chilena de Obstetricia y Ginecologia 53(3): 153-155
Horváth, M.; Tímár, L.; Karcagi, V.; Czeizel, E. 1997: The importance of molecular genetic diagnosis of Martin-Bell disease in genetic counseling Orvosi Hetilap 138(9): 541-545
Han, M.-y.; Huang, S.-s.; Wang, G.-j.; Yuan, Y.-y.; Kang, D.-y.; Zhang, X.; Dai, P. 2011: Prenatal genetic counseling and instruction for deaf families by genetic test Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 46(11): 909-913
James, D.C.; Crandall, L.A.; Rienzo, B.A.; Trottier, R.W. 1995: Roles of physicians, genetic counselors, and nurses in the genetic counseling process Journal of the Florida Medical Association 82(6): 403-410
Kumar, A.; Karan, S.; Waghrey, B.; Waghrey, V. 1978: A short case report of sirenomelia associated with the potter's syndrome Indian Pediatrics 15(12): 1049-1050
Prado, F.; Dos Ramos, J.P.; Larrañaga, N.; Espil, G.; Kozima, S. 2018: Solitary fibrous tumor and Doege-Potter syndrome Medicina 78(1): 47-49