Route Planning Based On Urban Mobility Management

Por Mátrai Tamás, Tóth János, Horváth Márton Tamás
Publicado em 2016-12-01

Rapid Trisomy Diagnosis (21, 18, and 13) Using Fluorescent PCR and Short Tandem Repeats: Applications for Prenatal Diagnosis and Preimplantation Genetic Diagnosis

Por Findlay, Ian, Tóth, Tamás, Matthews, Paul, Marton, Tamás, Quirke, Philip, Papp, Zoltán
Publicado em 1998

The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder

Por Hodgetts Morton, Victoria, Quinlan‐Jones, Elizabeth, Butts, Natasha, Williams, Denise, Hamilton, Sue, Marton, Tamas, Morris, Katie
Publicado no Clin Case Rep (2017)

Cardiac, bone and growth plate manifestations in hypocalcemic infants: revealing the hidden body of the vitamin D deficiency iceberg

Por Uday, Suma, Fratzl-Zelman, Nadja, Roschger, Paul, Klaushofer, Klaus, Chikermane, Ashish, Saraff, Vrinda, Tulchinsky, Ted, Thacher, Tom D., Marton, Tamas, Högler, Wolfgang
Publicado no BMC Pediatr (2018)

Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome

Por Morgan, Neil V., Brueton, Louise A., Cox, Phillip, Greally, Marie T., Tolmie, John, Pasha, Shanaz, Aligianis, Irene A., van Bokhoven, Hans, Marton, Tamas, Al-Gazali, Lihadh, Morton, Jenny E. V., Oley, Christine, Johnson, Colin A., Trembath, Richard C., Brunner, Han G., Maher, Eamonn R.
Publicado em 2006

Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)

Por Meyer, Esther, Ricketts, Christopher, Morgan, Neil V., Morris, Mark R., Pasha, Shanaz, Tee, Louise J., Rahman, Fatimah, Bazin, Anne, Bessières, Bettina, Déchelotte, Pierre, Yacoubi, Mohamed T., Al-Adnani, Mudher, Marton, Tamas, Tannahill, David, Trembath, Richard C., Fallet-Bianco, Catherine, Cox, Phillip, Williams, Denise, Maher, Eamonn R.
Publicado em 2010