List of bibliographic references
Number of relevant bibliographic references: 37.
[0-20] [
0 - 20][
0 - 37][
20-36][
20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 000081 (1999) |
D. Mowat [Australie] ; A. Jauch ; L. Robson ; A. Smith | Duplication within chromosome 5q characterized by fluorescence in situ hybridization. |
| 000221 (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. |
| 000260 (1999) |
A. Tsezou [Grèce] ; C. Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; E. Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani ; C. Theodoridis ; P C Patsalis ; N. Moschonas ; S. Kitsiou | Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy. |
| 000461 (2000) |
L. S Vendahl [Suède] ; M L Davenport | Delayed diagnoses of Turner's syndrome: proposed guidelines for change. |
| 000655 (2001) |
M. Sood [Inde] ; A. Trehan | Turner's syndrome in infancy. |
| 000754 (2001) |
C. Boucher ; C. Sargent ; T. Ogata ; N. Affara | Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location |
| 000833 (2001) |
M M Van Haelst [Pays-Bas] ; J. Hoogeboom ; R J Galjaard ; W J Kleijer ; N S Den Hollander ; R R De Krijger ; R C Hennekam ; M F Niermeijer | Lymphangiectasia with persistent Müllerian derivatives: confirmation of autosomal recessive Urioste syndrome. |
| 000B29 (2002) |
Inge D C. Van Balkom ; Mariel Alders ; Judith Allanson ; Carlo Bellini ; Ulrich Frank ; Greetje De Jong ; Ingeborg Kolbe ; Didier Lacombe ; Stan Rockson ; Peter Rowe ; Frits Wijburg ; Raoul C M. Hennekam | Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review. |
| 000E31 (2003) |
Anita Rauch [Allemagne] ; Maike Beese ; Ertan Mayatepek ; Helmut-Günther Dörr ; Dieter Wenzel ; André Reis ; Udo Trautmann | A novel 5q35.3 subtelomeric deletion syndrome. |
| 001A27 (2004) |
Mariam Patrícia Auada [Brésil] ; Maria Letícia Cintra ; Maria Beatriz Puzzi ; Danilo Viana ; Denise Pontes Cavalcanti | Scalp lesions in Turner syndrome: a result of lymphoedema? |
| 001B14 (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. |
| 001C31 (2005) |
Eugenio Bonioli [Italie] ; Raoul C. Hennekam ; Gianantonio Spena ; Guido Morcaldi ; Antonio Di Stefano ; Giovanni Serra ; Carlo Bellini | Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia. |
| 002024 (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. |
| 002374 (????) |
Emily M. Lambert [États-Unis] ; James Dziura ; Lynda Kauls ; Mark Mercurio ; Richard J. Antaya | Yellow nail syndrome in three siblings: a randomized double-blind trial of topical vitamin E. |
| 002540 (????) |
C. Severien ; S. Felix ; K. Bartholomé | Ring chromosome 22: a case report. |
| 002680 (1991) |
L. Zelante [Italie] ; F. Torricelli ; S. Calvano ; R. Mingarelli ; B. Dallapiccola | Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and review. |
| 002706 (1991) |
L G Kindblom [Suède] ; G. Stenman ; L. Angervall | Morphological and cytogenetic studies of angiosarcoma in Stewart-Treves syndrome. |
| 002852 (2007) |
Thomas Morgan [États-Unis] | Turner syndrome: diagnosis and management. |
| 002953 (2007) |
Anita Rauch [Allemagne] ; Helmuth-Günther Dörr | Chromosome 5q subtelomeric deletion syndrome. |
| 002A67 (????) |
D. Simm [Allemagne] ; K. Degenhardt ; C. Gerdemann ; T M K. Völkl ; A. Rauch ; H G Dörr | [Chronological age of patients with Turner syndrome at diagnosis]. |
| 003D12 (1991) |
S. Douvier ; J P Feldman ; A. Nivelon-Chevalier ; M. Degrolard ; M H Harran ; J. Jahier | [Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases]. |
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Ncbi/Curation
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Curation/Mesh.i -k "Karyotyping"
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Curation/Mesh.i \
-Sk "Karyotyping" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Curation/biblio.hfd
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Ncbi
|étape= Curation
|type= indexItem
|index= Mesh.i
|clé= Karyotyping
}}
| This area was generated with Dilib version V0.6.31.
Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024 |  |
