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Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome
Laila Rifai, Marylin Port-Lis, Anne-Claude Tabet, Isabelle Bailleul-Forestier, Brigitte Benzacken, Séverine Drunat, Suzanne Kuzbari, Sandrine Passemard, Alain Verloes, Azzedine AbouraVolume:
152A
Year:
2010
Language:
english
Pages:
7
DOI:
10.1002/ajmg.a.33164
File:
PDF, 202 KB
english, 2010