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American Journal of Medical Genetics|January 20, 1997
Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13A Tar, A Ion, J Sólyom, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 23, 2003
Mutational analysis of Hungarian patients with androgen insensitivity syndromeDóra Scheiber, Csaba Barta, Zita Halász, et al.
Thyroid : Official Journal of the American Thyroid Association|February 12, 2010
Hyperthyroidism caused by a germline activating mutation of the thyrotropin receptor gene: difficulties in diagnosis and therapyRita Bertalan, Agnes Sallai, János Sólyom, et al.
Fetal Diagnosis and Therapy|June 16, 2001
Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplificationM Theodoropoulou, C Barta, M Szoke, et al.
The Journal of Clinical Endocrinology and Metabolism|July 15, 1999
Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasiaA Ferenczi, M Garami, E Kiss, et al.
Orvosi Hetilap|October 27, 1997
[Androgen-producing adrenocortical adenoma in childhood. Pitfalls of differential diagnosis]K Gyulay, T Niederland, G Rudas, et al.
Orvosi Hetilap|August 10, 2007
[Mixed gonadal dysgenesis associated with an isodicentric Y chromosome]László Ságodi, Enikô Sólyom, András Tóth, et al.
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