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Mackay D.J.(undefined)Epimutations in Prader—Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect undefined undefined undefined-undefined
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Hahnemann J.M.(undefined)Mosaic maternal uniparental disomy of chromosome 15 in Prader—Willi syndrome: utility of genome-wide SNP array undefined undefined undefined-undefined
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Messerschmidt D.M.(undefined)Mosaic imprinting defect in a patient with an almost typical expression of the Prader—Willi syndrome undefined undefined undefined-undefined
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de Vries W.(undefined)Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype undefined undefined undefined-undefined
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Ito M.(undefined)The origin of imprinting defects in Temple syndrome and comparison with other imprinting disorders undefined undefined undefined-undefined
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Smith Z.D.(undefined)Quantification of the methylation at the undefined undefined undefined-undefined
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Meissner A.(undefined) locus identifies subtypes of sporadic pseudohypoparathyroidism type undefined undefined undefined-undefined
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Plasschaert R.N.(undefined)Mosaicism for undefined undefined undefined-undefined
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Bartolomei M.S.(undefined) methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases undefined undefined undefined-undefined
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Fuke-Sato T.(undefined)Recent advances in imprinting disorders undefined undefined undefined-undefined