| symptoms < syndrome < syndromes | Facettes : |
List of bibliographic references
Number of relevant bibliographic references: 3.| Ident. | Authors (with country if any) | Title |
|---|---|---|
| 000210 (2005) | T. Hienonen [Finlande] ; H. Sammalkorpi [Finlande] ; P. Isohanni [Finlande] ; R. Versteeg [Pays-Bas] ; R. Karikoski [Finlande] ; L A Aaltonen [Finlande] | A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma |
| 000636 (1995) | Louise Telvi [France] ; Alain Bernheim [France] ; Alexandra Ion ; Françoise Fouquet ; Yves Le Bouc [France] ; Jean-Louis Chaussain | Gonadal dysgenesis in del(18p) syndrome |
| 000659 (1994) | Junko Oshima [Canada] ; Chang-En Yu [Canada] ; Michael Boehnke [Canada] ; James L. Weber [Canada] ; Susanne Edelhoff [Canada] ; Michael J. Wagner [Canada] ; Dan E. Wells [Canada] ; Stephen Wood [Canada] ; Christine M. Disteche [Canada] ; George M. Martin [Canada] ; Gerard D. Schellenberg [Canada] | Integrated Mapping Analysis of the Werner Syndrome Region of Chromosome 8 |
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