J. Huber

Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: Case report and review of literature

J. Squire, A. C. Laus, W. Baratela, 2012, American journal of medical genetics. Part A.

Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies.

R. Ferriani, J. Huber, E. Ramos, 2009, Molecular human reproduction.

The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma.

J. Huber, E. Ramos, E. S. Ramos, 2006, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations

W. A. Silva, J. Huber, L. F. Araujo, 2019, The International journal of biological markers.

Investigation of IGF2/ApaI and H19/RsaI polymorphisms in patients with cutaneous melanoma.

J. Huber, E. Ramos, Á. Rios, 2010, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Velocardiofacial syndrome with a rare t(2;22).

J. Huber, E. Ramos, M. V. Gomes, 2007, Clinical dysmorphology.

Fuhrmann syndrome: two Brazilian cases

J. Huber, J. Volpon, E. Ramos, 2003, Clinical Dysmorphology.

Karyotype-phenotype-genotype correlation in a 4p;12q rearrangement

J. Squire, A. Gomes, S. A. Santos, 2015 .