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L Bondeson

Showing results (71-80 of 77) with videos related to

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International Journal of Cancer|January 27, 1997
Karyotypic abnormalities in fibroadenomas of the breastC Petersson, N Pandis, H Rizou, et al.
Human Molecular Genetics|March 1, 1997
Molecular and phenotypic variation in patients with severe Hunter syndromeK M Timms, M L Bondeson, M A Ansari-Lari, et al.
Journal of Medical Genetics|May 6, 2008
Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disordersA-M Nyström, S Ekvall, E Berglund, et al.
Genes, Chromosomes & Cancer|May 23, 1998
Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patientsN Pandis, M R Teixeira, A Adeyinka, et al.
Annals of Human Genetics|February 3, 2009
Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populationsA Konings, L Van Laer, A Wiktorek-Smagur, et al.
Journal of Medical Genetics|December 20, 2011
A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial featuresAnna-Maja Molin, J Andrieux, D A Koolen, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
International Journal of Cancer|January 27, 1997
Karyotypic abnormalities in fibroadenomas of the breastC Petersson, N Pandis, H Rizou, et al.
Human Molecular Genetics|March 1, 1997
Molecular and phenotypic variation in patients with severe Hunter syndromeK M Timms, M L Bondeson, M A Ansari-Lari, et al.
Journal of Medical Genetics|May 6, 2008
Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disordersA-M Nyström, S Ekvall, E Berglund, et al.
Genes, Chromosomes & Cancer|May 23, 1998
Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patientsN Pandis, M R Teixeira, A Adeyinka, et al.
Annals of Human Genetics|February 3, 2009
Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populationsA Konings, L Van Laer, A Wiktorek-Smagur, et al.
Journal of Medical Genetics|December 20, 2011
A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial featuresAnna-Maja Molin, J Andrieux, D A Koolen, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 8