مکتبة رقمیه للعلوم الطبيه
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  2. Details for: Human imprinting syndromes.
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Human imprinting syndromes. [electronic resource]

By:
  • Lim, Derek Hk
Contributor(s):
  • Maher, Eamonn R
Producer: 20120416Description: 347-69 p. digitalISSN:
  • 1750-192X
Subject(s):
  • Adaptor Proteins, Signal Transducing -- genetics
  • Angelman Syndrome -- genetics
  • Beckwith-Wiedemann Syndrome -- genetics
  • Chromosome Disorders -- genetics
  • Chromosomes, Human, Pair 11 -- genetics
  • Chromosomes, Human, Pair 14 -- genetics
  • Chromosomes, Human, Pair 15 -- genetics
  • Chromosomes, Human, Pair 20 -- genetics
  • Chromosomes, Human, Pair 6 -- genetics
  • Diabetes Mellitus -- genetics
  • Female
  • Fibrous Dysplasia, Polyostotic -- genetics
  • Genomic Imprinting -- physiology
  • Humans
  • Hydatidiform Mole -- genetics
  • Multigene Family -- genetics
  • Mutation -- genetics
  • Prader-Willi Syndrome -- genetics
  • Pregnancy
  • Pseudohypoparathyroidism -- genetics
  • Silver-Russell Syndrome -- genetics
  • Uniparental Disomy -- genetics
Online resources:
  • Available from publisher's website
In: Epigenomics vol. 1
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Publication Type: Journal Article; Review

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Human imprinting syndromes.

APA

Lim D. H., Maher E. R., . (20120416). Human imprinting syndromes. : Epigenomics.

Chicago

Lim Derek Hk, Maher Eamonn R, . 20120416. Human imprinting syndromes. : Epigenomics.

Harvard

Lim D. H., Maher E. R., . (20120416). Human imprinting syndromes. : Epigenomics.

MLA

Lim Derek Hk, Maher Eamonn R, . Human imprinting syndromes. : Epigenomics. 20120416.

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