| 6. |
D Obler, A L Juraszek, L B Smoot, M R Natowicz |
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Double outlet right ventricle: aetiologies and associations |
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J. Med. Genet. 2008; 45: 481-497.
(In "Reviews")
[Abstract]
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H F A Vasen, G Möslein, A Alonso, I Bernstein, L Bertario, I Blanco, J Burn, G Capella, C Engel, I Frayling, W Friedl, F J Hes, S Hodgson, J-P Mecklin, P Møller, F Nagengast, Y Parc, L Renkonen-Sinisalo, J R Sampson, A Stormorken, J Wijnen |
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Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer) |
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J. Med. Genet. 2007; 44: 353-362.
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[Abstract]
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| 8. |
S M Park, V K K Chatterjee |
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Genetics of congenital hypothyroidism |
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J. Med. Genet. 2005; 42: 379-389.
(In "Reviews")
[Abstract]
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| 9. |
P de Bie, P Muller, C Wijmenga, L W J Klomp |
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Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes |
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J. Med. Genet. 2007; 44: 673-688.
(In "Reviews")
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| 10. |
Carla Lintas, Antonio M Persico |
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Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist |
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J. Med. Genet. 2008; doi: 10.1136/jmg.2008.060871.
(In "Review article")
[Abstract]
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