Identification of Nine Novel Mutations in the Hepatocyte Nuclear Factor 1 Alpha Aene Associated with Maturity-Onset Diabetes of the Young (MODY3)

By Vaxillaire Martine   Rouard Mathias   Yamagata Kazuya   Oda Naohisa   Kaisaki Pamela J.   Boriraj V. Vicky   Chevre Jean-Claude   Boccio Valérie   Cox Roger D.   Lathrop G. Mark   Dussoix Philippe   Philippe Jacques   Timsit José   Charpentier Guillaume   Velho Gilberto   Bell Graeme I.   Froguel Philippe  

Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 583-586

Oxford University Press

Access to resources Recommend Favorite

Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease

By  

Molecular Genetics & Genomic Medicine, Vol. 3, Iss. 5, 2015-09 ,pp. : 413-423

John Wiley & Sons Inc

Access to resources Recommend Favorite

Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease

By  

Molecular Genetics & Genomic Medicine, Vol. 2324-9269, Iss. 5, 2015-09 ,pp. : 413-423

John Wiley & Sons Inc

Access to resources Recommend Favorite

Neonatal diabetes mellitus due to a novel mutation in the GATA6 gene accompanying renal dysfunction: A case report

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 4, 2015-04 ,pp. : 925-927

John Wiley & Sons Inc

Access to resources Recommend Favorite

Germline hepatocyte nuclear factor 1α and 1 mutations in renal cell carcinomas

By Rebouissou Sandra  

Human Molecular Genetics, Vol. 14, Iss. 5, 2005-03 ,pp. : 603-614

Oxford University Press

Access to resources Recommend Favorite