Waardenburg's syndrome. a familial case relating to 4 generations and 23 individuals
Roux, C.; Baheux, G.; Gaulier, M.; Caldera, R.; Soepardan, L.
Annales de Genetique 13(2): 125-128
1970
ISSN/ISBN: 0003-3995 PMID: 5310696 Document Number: 19784
Document emailed within 1 workday
Related Documents
Poissonnier, M.; Andrieu, J.; Gardon, J.D.; Saint-Martin, J.L.; Gruyer, P.; Martignon, C. 1983: Familial cancer of the colon without polyposis and the familial cancer syndrome. Apropos of 2 cases over 3 generations Journal de Genetique Humaine 31(4): 255-278Dubosson, J.D.; Klein, D.; Pettavel, J.; Rey, C.H. 1977: Familial cancer syndrome studies in 4 generations of a family Schweizerische Medizinische Wochenschrift 107(25): 875-881
Ferrández, A.; Remírez, J.; Sáenz, P.; Calvo, M. 1980: The trichorhinophalangeal syndrome. Report of 4 familial cases belonging to 4 generations Helvetica Paediatrica Acta 35(6): 559-567
Patrizi, A.; Colombati, S.; Valenti, L. 1985: A case of Waardenburg-Klein syndrome Giornale Italiano di Dermatologia e Venereologia: Organo Ufficiale Societa Italiana di Dermatologia e Sifilografia 120(4): 277-279
Aritürk, E.; Tosyali, N.; Aritürk, N. 1992: A case of Waardenburg syndrome and aganglionosis Turkish Journal of Pediatrics 34(2): 111-114
Demirci, G.Tukenmez.; Atıs, G.; Altunay, I.Kıvanc. 2011: Waardenburg Syndrome type 1: A case report Dermatology Online Journal 17(11): 3
Rebaud, P.; David, L.; Plauchu, H.; Chatelain, P.; Moulin, G.; François, R. 1985: A familial case of Rothmund-Thomson syndrome. A case in favor of the uniqueness of the syndrome. Association with osteosarcoma Pediatrie 40(6): 487-492
Yalaburgi, S.B.; Mistry, P.K. 1979: Waardenburg's syndrome Central African Journal of Medicine 25(9): 200-201
Stoll, C.; Alembik, Y.; Dott, B. 1999: Familial coarctation of the aorta in three generations Annales de Genetique 42(3): 174-176
Sarin, Y.K.; Manchanda, V. 2006: Shah Waardenburg syndrome Indian Pediatrics 43(5): 452
Stelmasiak, Z.; Rozynkowa, D. 1973: Familial osteosclerosis associated with facial hemispasm in 3 generations Polski Tygodnik Lekarski 28(21): 774-776
Hageman, M.E. 1974: The Waardenburg syndrome in tropical Africa Nederlands Tijdschrift Voor Geneeskunde 118(37): 1393-1396
Hussels, I.E. 1971: Vitiligo versus Waardenburg syndrome Birth Defects Original Article Series 7(8): 285
Dastur, Y.K.; Dudhani, A.; Chitale, A.; Dasgupta, S. 1995: Waardenburg syndrome with anisocoria and exotropia Journal of Postgraduate Medicine 41(4): 111-112
Walter-Roşianu, A. 1985: Bourneville's tuberous sclerosis (a familial study of 3 generations) Revista de Pediatrie Obstetrica Si Ginecologie. Pediatria 34(1): 53-62
Centerwall, W.; Francke, U. 1977: Familial trisomy 20p five cases and two carriers in three generations a review Annales de Genetique 20(2): 77-83
Ibsen, H.H.; Clemmensen, O.J.; Brandrup, F. 1991: Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations Acta Dermato-Venereologica 71(4): 349-351
MacEwen, G.D.; Zaharko, W. 1973: Multiple lentigines syndrome. A case report of a rare familial syndrome with orthopaedic considerations Clinical Orthopaedics and Related Research 1973(97): 34-37
Tasdemir, S.; Erdem, H.B.; Sahin, I.; Kara, M.; Tatar, A. 2015: Waardenburg Syndrome type 1 and a Rare Finding of Anal Atresia Genetic Counseling 26(4): 467-470
Koifman, R.J.; Koifman, S.; Vieira, R.J. 1998: Familial aggregation of breast/ovarian cancer: age of onset along subsequent generations in Brazil Cadernos de Saude Publica 14(Suppl 3): 181-185