S. Dória

H. Guimarães, G. Rocha, F. Flôr-de-Lima, 2017, Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology.

Clinical outcomes of 77 TESE treatment cycles in non-mosaic Klinefelter syndrome patients

M. Sousa, S. Dória, M. Cunha, 2021, JBRA assisted reproduction.

Treatment by testicular sperm extraction and intracytoplasmic sperm injection of 65 azoospermic patients with non‐mosaic Klinefelter syndrome with birth of 17 healthy children

A. Barros, F. Carvalho, M. Sousa, 2014, Andrology.

Aneuploidies detection in miscarriages and fetal deaths using multiplex ligation-dependent probe amplification: an alternative for speeding up results?

M. Sousa, A. Matias, A. Barros, 2010, European journal of obstetrics, gynecology, and reproductive biology.

Chromosome mis-segregation and cytokinesis failure in trisomic human cells

Darawalee Wangsa, Thomas Ried, Jordi Camps, 2015, eLife.

Altered expression of epigenetic regulators and imprinted genes in human placenta and fetal tissues from second trimester spontaneous pregnancy losses

S. Dória, C. Ramalho, S. Vasconcelos, 2019, Epigenetics.

Identification of Copy Number Variation by Array-CGH in Portuguese Children and Adolescents Diagnosed with Autism Spectrum Disorders

M. Leão, S. Dória, J. Pinto, 2019, Neuropediatrics.

An efficient protocol for the detection of chromosomal abnormalities in spontaneous miscarriages or foetal deaths.

M. Sousa, A. Matias, A. Barros, 2009, European journal of obstetrics, gynecology, and reproductive biology.

Normal sperm in a 2;2 homologous male translocation carrier

A. Barros, S. Dória, C. Almeida, 2012, Journal of Assisted Reproduction and Genetics.

Prenatal diagnosis: the clinical usefulness of array comparative genomic hybridization

S. Dória, C. Ramalho, J. Pinto, 2018, Porto biomedical journal.

Copy number variations on chromosome 2: impact on human phenotype, a cross-sectional study

A. Grangeia, S. Dória, J. Pinto, 2023, Porto biomedical journal.

Intellectual disability and overgrowth—A new case of 19p13.13 microdeletion syndrome with digital abnormalities

M. Leão, S. Dória, Rita Jorge, 2015, American journal of medical genetics. Part A.

X-chromosome inactivation: implications in human disease

G. Pereira, S. Dória, 2021, Journal of Genetics.

46,XX male disorder of sexual development

M. Fontoura, S. Dória, C. Castro-Correia, 2020, Clinical Pediatric Endocrinology.

Expression and function of sodium transporters in two opossum kidney cell clonal sublines.

Jing Xu, P. Jose, P. Soares-da-Silva, 2002, American journal of physiology. Renal physiology.

Frequency of NUP98-NSD1 fusion transcript in childhood acute myeloid leukaemia

M. Teixeira, S. Castedo, B. Borges, 2003, Leukemia.

Prenatal diagnosis study using array comparative genomic hybridization for genotype-phenotype correlation in 772 fetuses.

A. Grangeia, S. Dória, C. Ramalho, 2022, Annals of diagnostic pathology.

Late-onset Lennox-Gastaut syndrome as a phenotype of 15q11.1q13.3 duplication

M. Rosas, Renata Oliveira, S. Dória, 2012, Epileptic disorders.

Detection of prognostic significant translocations in childhood acute lymphoblastic leukaemia by one‐step multiplex reverse transcription polymerase chain reaction

S. Castedo, N. Cerveira, I. Veiga, 2000, British journal of haematology.

Phenotypic Expression in the First Case of Complete Trisomy 12: Combination of Prenatal Ultrasound and Necropsic Examination

J. Oliveira, A. Matias, S. Dória, 2009, Fetal Diagnosis and Therapy.

Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses

M. Sousa, A. Barros, F. Carvalho, 2010, Journal of Assisted Reproduction and Genetics.

12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?

M. Pinho, M. Leão, S. Dória, 2020, BMC Medical Genomics.

Clinicopathological features of 45,X/46,Xidic(Y) mosaicism and therapeutic implications: case report.

J. Lopes, M. Fontoura, Henrique Soares, 2008, Sao Paulo medical journal = Revista paulista de medicina.

Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage.

C. Morton, Joana Fino, D. David, 2023, Gene.

The role of DNA hydroxymethylation and TET enzymes in placental development and pregnancy outcome

S. M. Chuva de Sousa Lopes, S. Dória, Carla Caniçais, 2023, Clinical Epigenetics.

Klinefelter syndrome: The characterization of the clinical and sociological features of 51 patients.

S. Souto, S. Dória, D. Carvalho, 2023, Revista internacional de andrologia.

Late-onset Lennox-Gastaut syndrome as a phenotype of 15q11.1q13.3 duplication

M. Rosas, Renata Oliveira, S. Dória, 2012, Epileptic disorders : international epilepsy journal with videotape.