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Multiple genomic aberrations in a patient with mental retardation and hypogonadism: 45,X/46,X,psu dic(Y) karyotype, thyroid hormone receptor beta (THRB) mutation and heterozygosity for Wilson disease. [electronic resource] by
- Hes, Frederik J
- Madan, Kamlesh
- Rombout-Liem, I Shan
- Szuhai, Karoly
- Sørensen, Helena
- van Amstel, Hans Kristian Ploos
- Bakker, Egbert
- Visser, Theo J
- Smit, Johannes W
- Hansson, Kerstin
Producer: 20091217
In:
American journal of medical genetics. Part A vol. 149A
Availability: No items available.
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