Type C hereditary brachydactyly. Clinical and genetic study of 3 families
Gnamey, D.; Walbaum, R.; Saint-Aubert, P.; Fontaine, G.
Annales de Pediatrie 18(6): 438-449
1971
ISSN/ISBN: 0066-2097 PMID: 5564915 Document Number: 34916
Document emailed within 1 workday
Related Documents
Gnamey, D.; Walbaum, R.; Fontaine, G. 1977: Study of fingerprints in 12 cases of hereditary brachydactyly type C and e Journal de Genetique Humaine 25(4): 279-289Lorenzo Sanz, G.; Barrios Castellanos, R.; Quintana Castilla, A.; Corbatón Blasco, J.; García Lacalle, C. 1989: Type C hereditary brachydactyly Revista Clinica Espanola 184(3): 139-142
Lei, W.-T.; Shyur, S.-D.; Huang, L.-H.; Kao, Y.-H.; Lo, C.-Y. 2011: Type i hereditary angioedema in Taiwan -- clinical, biological features and genetic study Asian Pacific Journal of Allergy and Immunology 29(4): 327-331
Morales Asin, F.; Mostacero Miguel, E.; García Alvarez, F.; Olascoaga Urtaza, J.; Domínguez Arranz, M.; Morales Asin, J.; López del Val, J. 1980: Clinical study of 8 families with various members affected with myotonic dystrophy of Curshmann Steinert's type. Genetic considerations Revista Clinica Espanola 157(5): 319-323
Von Fellenberg, J.; Paternotte, C.; Prud'homme, J.F.; Weissenbach, J.; Hazan, J.; Burgunder, J.M. 1998: Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis Schweizerische Medizinische Wochenschrift 128(26): 1043-1050
Schwartz, M.; Nørby, S.; Brandt, N.J. 1985: DNA markers, genetic counseling and prenatal diagnosis of hereditary disease. a study of 3 families with Duchenne's muscular dystrophy Ugeskrift for Laeger 147(26): 2071-2075
Sharkova, I.V.; Milovidova, T.B.; Dadali, E.L.; Poliakov, A.V. 2012: Clinical-genetic characteristics of hereditary motor-sensory neuropathy type 1 X Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 112(7): 42-47
Alonso, M.E.; Barbosa, S.; Zúñiga, M.; Smith, P.; Fernández, A.; García Ramos, G.; Lozano, D. 1987: Dystrophia myotonica. Clinical and genetic study of 21 cases in 18 families Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 39(2): 155-162
Rebollar Mesa, J.L. 1975: Hereditary brachydactyly Revista Clinica Espanola 136(2): 169-172
Galina, K.P.; Peresun'ko, A.P.; Glushchenko, N.N. 2001: Clinical genealogy and genetic-mathematical study of families of probands with uterine cancer in the Chernovitsy Region Tsitologiia i Genetika 35(2): 26-29
La Rocca, E.; Amoroso, S.; Brai, M.; Di Leonardo, S.; Aricò, M. 1986: Hereditary angioedema. Genealogic studies and clinical considerations on 2 genetic forms in a case study of 10 patients Giornale Italiano di Dermatologia e Venereologia: Organo Ufficiale Societa Italiana di Dermatologia e Sifilografia 121(3): 203-208
Cuevas-Sosa, A.; García-Segur, F. 1971: Brachydactyly with absence of middle phalanges and hypoplastic nails. a new hereditary syndrome Journal of Bone and Joint Surgery. British Volume 53(1): 101-105
Spiegel, R.; Mächler, M.; Stocker, H.P.; Boltshauser, E.; Schmid, W. 1991: Neurofibromatosis Type 1: genetic studies with DNA markers in 38 families Schweizerische Medizinische Wochenschrift 121(40): 1445-1452
Svendsen, I.H.; Steensgaard-Hansen, F.; Nordvåg, B.Y. 1999: Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. a clinical, genetic and echocardiographic study of an affected Danish family Ugeskrift for Laeger 161(36): 4995-4999
Meire, G.M.; Cochaux, P.; Candaele, C.; Broux, C. 1994: Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON) Bulletin de la Societe Belge d'Ophtalmologie 254: 137-146
Sanz, J.; Gilgenkrantz, S. 1988: Type C brachydactyly transmitted through four generations Annales de Genetique 31(1): 43-46
Broekmans, A.W.; Bertina, R.M.; Reinalda-Poot, J.; Engesser, L.; Muller, H.P.; Leeuw, J.A.; Michiels, J.J.; Brommer, E.J.; Briët, E. 1985: Hereditary protein S deficiency and venous thrombo-embolism. a study in three Dutch families Thrombosis and Haemostasis 53(2): 273-277
Novikov, V.P.; Stefanenko, G.N.; Ignat'ev, I.T.; Morova, N.A. 1987: 2 cases of peculiar manifestation of type e brachydactyly Klinicheskaia Meditsina 65(3): 144-145
Tanaka, K. 1974: Genetic study of hereditary nephritis Nihon Jinzo Gakkai Shi 16(6): 624-628
Likhtenshteĭn, V.A.; Mugutdinov, T.M.; Solomianskiĭ, A.E. 1977: Clinical and genetic aspects of hereditary acro-osteolysis Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 77(10): 1452-1458