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Orvosi Hetilap|June 1, 2006
[Novel approaches to the background of developmental abnormalities: clinical genetics of transcription factors]Alexandra Tészás, Judit Kárteszi, György KosztolányiFrontiers in Pediatrics|September 7, 2021
Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the FOXP2 GeneOrsolya Nagy, Judit Kárteszi, Beatrix Elmont, et al.Orvosi Hetilap|February 23, 2025
[Duplication of the X-chromosomal Xq28 region containing the MECP2 gene in X-linked intellectual disability syndrome Lubs-type]Zsófia Németh, Gabriella Sinkó, Judit Kárteszi, et al.American Journal of Medical Genetics. Part A|December 28, 2002
Clinical and genetic heterogeneity in frontometaphyseal dysplasia: severe progressive scoliosis in two familiesEva Morava, Tamás Illés, János Weisenbach, et al.Clinical Dysmorphology|December 1, 2005
Transient progeroid phenotype and lipodystrophy in mosaic polyploidyJudit Kárteszi, György Kosztolányi, Marta Czakó, et al.Clinical Dysmorphology|October 18, 2003
Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndromeEva Morava, Marta Czakó, Judit Kárteszi, et al.European Journal of Pediatrics|November 9, 2002
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasiaEva Morava, Judit Kárteszi, János Weisenbach, et al.Orvosi Hetilap|March 21, 2008
[Psychological aspects of presymptomatic diagnosis in Huntington disease]Berta Bondor, Judit Kárteszi, Kinga Hadzsiev, et al.Clinical Dysmorphology|July 19, 2003
Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotoniaEva Morava, Oliver Bartsch, Márta Czakó, et al.Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|July 28, 2004
Screening for CDG type Ia in Joubert syndromeEva Morava, Beatrix Cser, Judit Kárteszi, et al.Pageof 2