NR0B1 (DAX1) mutations in patients affected by congenital adrenal hypoplasia with growth hormone deficiency as a new finding

• Autorzy: Rojek A. , Obara-Moszynska M. , Malecka E. , Slomko-Jozwiak M. , Niedziela M.
• Języki publikacji: EN
• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2013
• Tom: 54
• Numer: 2
• Opis fizyczny: p.225–230,fig.,ref.

Twórcy

autor

Rojek A.

• Molecular Endocrinology Laboratory, 2nd Chair of Pediatrics, Department of Pediatric Endocrinology and Rheumatology, Poznan University of Medical Sciences, Szpitalna 27/33 Street, 60-572 Poznan, Poland

autor

Obara-Moszynska M.

• 2nd Chair of Pediatrics, Department of Pediatric Endocrinology and Rheumatology, Poznan University of Medical Sciences, Szpitalna Street 27/33, 60-572 Poznan, Poland

autor

Malecka E.

• Department of Pediatric Endocrinology and Rheumatology, Karol Jonscher's Clinical Hospital, Szpitalna Street 27/33, 60-572 Poznan, Poland

autor

Slomko-Jozwiak M.

• Department of Pediatric Endocrinology and Rheumatology, Karol Jonscher's Clinical Hospital, Szpitalna Street 27/33, 60-572 Poznan, Poland

autor

Niedziela M.

• Molecular Endocrinology Laboratory, 2nd Chair of Pediatrics, Department of Pediatric Endocrinology and Rheumatology, Poznan University of Medical Sciences, Szpitalna Street 27/33, 60-572 Poznan, Poland

Uwagi

PL

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