𝔖 Bobbio Scriptorium
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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

✍ Scribed by Frederik J. Hes; Kamlesh Madan; I. Shan Rombout-Liem; Karoly Szuhai; Helena Sørensen; Hans Kristian Ploos van Amstel; Egbert Bakker; Theo J. Visser; Johannes W. Smit; Kerstin Hansson


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
109 KB
Volume
149A
Category
Article
ISSN
1552-4825

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