List of bibliographic references indexed by Syndrome de Turner (génétique)
Number of relevant bibliographic references: 36.
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| Ident. | Authors (with country if any) | Title |
|---|
| 000195 (2017) |
Agnieszka Frelich ; Jakub Frelich ; Wacław Je ; Tomasz Irzyniec [Pologne] | Selected clinical features of the head and neck in women with Turner syndrome and the 45,X/46,XY karyotype. |
| 001707 (2015) |
Giles Atton [Royaume-Uni] ; Kristiana Gordon [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Vaughan Keeley [Royaume-Uni] ; Katie Riches [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni] ; Peter Mortimer (dermatologue) [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] | The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review |
| 001A92 (2015) |
Sarar Mohamed ; Edna F. Roche ; Hilary M C V. Hoey | Mode of initial presentation and chromosomal abnormalities in Irish patients with Turner syndrome: a single-centre experience. |
| 003800 (2013) |
H T El-Bassyouni [Égypte] ; A. El-Gerzawy ; O. Eid ; M O El-Ruby | Clinical and cytogenetic study of a non mosaic 46, X, isodicentric Yq in an Egyptian patient with Turner syndrome. |
| 004406 (2012) |
Jolanta Wierzba [Pologne] ; María Concepci N Gil-Rodríguez [Espagne] ; Anna Polucha [Pologne] ; Beatriz Puisac [Espagne] ; María Arnedo [Espagne] ; María Esperanza Teresa-Rodrigo [Espagne] ; Dorota Winnicka [Pologne] ; Fausto G. Hegardt [Espagne] ; Feliciano J. Ramos [Espagne] ; Janusz Limon [Pologne] ; Juan Pié [Espagne] | Cornelia de Lange syndrome with NIPBL mutation and mosaic Turner syndrome in the same individual |
| 005591 (2010) |
Rosa Fernandez [Espagne] ; Eduardo Pasaro | Tall stature and gonadal dysgenesis in a non-mosaic girl 45,X. |
| 006876 (2008) |
Melissa L. Loscalzo [États-Unis] | Turner syndrome. |
| 006C20 (2008) |
Carolyn A. Bondy | Aortic Dissection in Turner Syndrome |
| 007012 (2007) |
S. Cabrol [France] | [Turner syndrome]. |
| 007061 (2007) |
Thomas Morgan [États-Unis] | Turner syndrome: diagnosis and management. |
| 007A56 (2006) |
K L Lachlan [Royaume-Uni] ; S. Youings ; T. Costa ; P A Jacobs ; N S Thomas | A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions. |
| 007E91 (2005) |
A. Debeer [Belgique] ; E. Steenkiste ; K. Devriendt ; M. Morren | Scalp skin lesion in Turner syndrome: more than lymphoedema? |
| 008043 (2005) |
Melissa L. Loscalzo [États-Unis] ; Phillip L. Van ; Vincent B. Ho ; Vladimir K. Bakalov ; Douglas R. Rosing ; Carol A. Malone ; Harry C. Dietz ; Carolyn A. Bondy | Association between fetal lymphedema and congenital cardiovascular defects in Turner syndrome. |
| 008689 (2004) |
Eve J. Lowenstein [États-Unis] ; Karen H. Kim ; Sharon A. Glick | Turner's syndrome in dermatology. |
| 008795 (2004) |
Valeria Brazzelli [Italie] ; Daniela Larizza ; Miriam Martinetti ; Sara Martinoli ; Valeria Calcaterra ; Annalisa De Silvestri ; Roberta Pandolfi ; Giovanni Borroni | Halo nevus, rather than vitiligo, is a typical dermatologic finding of turner's syndrome: clinical, genetic, and immunogenetic study in 72 patients. |
| 009953 (2001) |
M. Sood [Inde] ; A. Trehan | Turner's syndrome in infancy. |
| 009976 (2001) |
K A Leppig [États-Unis] ; C M Disteche | Ring X and other structural X chromosome abnormalities: X inactivation and phenotype. |
| 009E36 (2001) |
Marika J. Karkkainen [Finlande] ; Lotta Jussila [Finlande] ; Kari Alitalo [Finlande] ; Robert E. Ferrell ; David N. Finegold | Molecular regulation of lymphangiogenesis and targets for tissue oedema |
| 00A031 (2001) |
Catherine A. Boucher ; Carole A. Sargent ; Tsutomu Ogata ; Nabeel A. Affara | Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location [Original article] [Original article] |
| 00A729 (2000) |
Lars S Vendahl [États-Unis] ; Marsha L. Davenport [États-Unis] | Delayed diagnoses of Turner’s syndrome: Proposed guidelines for change |
| 00AA12 (1999) |
F. Haverkamp [Allemagne] ; J. Wölfle ; K. Zerres ; O. Butenandt ; P. Amendt ; B P Hauffa ; E. Weimann ; M. Bettendorf ; E. Keller ; R. Mühlenberg ; C J Partsch ; W G Sippell ; C. Hoppe | Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure. |
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