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congenital thyroid aplasia
(phenotype)
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Genetic Markers
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No genes found
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OMIM - Congenital disorder
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Abnormal fetal heart rate tracings and congenital fetal hypothyroidism.
Congenital unilateral aplasia of the thyroid lobe].
Congenital familial thyroid aplasia.
Congenital absence of the thyroid gland as a cause of Debré-Semelaigne syndrome].
The course of pregnancy in congenital thyroid gland aplasia. Case report with special reference to m…
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Incidence of cCPHD in Denmark - a National Observational Study
Chinese Medicine(Hu Yang Yang Kun Formula) for Primary Ovarian Insufficiency
Folic Acid and Zinc Supplementation Trial (FAZST)
A Study of KN046 in Patients With Thymic Carcinoma Who Failed Immune Checkpoint Inhibitors
European Union Registry in Paediatric Chronic Kidney Disease Patients Looking at Safety and Usage Pa…
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