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A rare case of 46,XX gonadal dysgenesis, Mayer–Rokitansky–K..:
Ambachew, Rediet
;
Gulilat, Amare
;
Aberra, Tewodros
...
Endocrinology, Diabetes & Metabolism Case Reports. 2022 (2022) - p. , 2022
Link:
https://doi.org/10.1530/edm-21-0103
RT Journal T1
A rare case of 46,XX gonadal dysgenesis, Mayer–Rokitansky–Kuster–Hauser syndrome, pituitary and thyroid hypoplasia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1530_edm-21-0103&Exemplar=1&LAN=DE A1 Ambachew, Rediet A1 Gulilat, Amare A1 Aberra, Tewodros A1 Terefework, Zewdu A1 Bedilu, Wubalem A1 Tarekegn, Getahun A1 Reja, Ahmed PB Bioscientifica YR 2022 SN 2052-0573 JF Endocrinology, Diabetes & Metabolism Case Reports VO 2022 LK http://dx.doi.org/https://doi.org/10.1530/edm-21-0103 DO https://doi.org/10.1530/edm-21-0103 SF ELIB - SuUB Bremen
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