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The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization
Author(s) -
Fukushima Yoshimitsu,
Ohashi Hirofumi,
Hasegawa Tomonobu
Publication year - 1993
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1993.tb03843.x
Subject(s) - ectrodactyly , ectodermal dysplasia , fluorescence in situ hybridization , medicine , in situ hybridization , anatomy , dermatology , biology , genetics , gene , chromosome , gene expression
Clin Genet 1993: 44: 50. © Munksgaard, 1993