[HTML][HTML] Novel homozygous mutation in the human RAX homeobox gene in a patient with bilateral anophthalmia and severe endocrine dysfunction – a case report …
YHA El-Nahry, V Bardinet, C Bührer… - Case Reports in …, 2024 - degruyter.com
Objectives Childhood visual impairment due to congenital malformation leads to severe
handicaps and lifelong consequences for the affected child. Congenital anophthalmia …
handicaps and lifelong consequences for the affected child. Congenital anophthalmia …
Novel homozygous mutation in the human RAX homeobox gene in a patient with bilateral anophthalmia and severe endocrine dysfunction–a case report and …
YHA El-Nahry, V Bardinet, C Bührer, W Henrich - degruyter.com
Objectives: Childhood visual impairment due to congenital malformation leads to severe
handicaps and lifelong consequences for the affected child. Congenital anophthalmia …
handicaps and lifelong consequences for the affected child. Congenital anophthalmia …