The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization

Yoshimitsu Fukushima; Tomonobu Hasegawa

doi:10.1111/j.1399-0004.1993.tb03843.x

The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization

Yoshimitsu Fukushima, Tomonobu Hasegawa

Research output: Contribution to journal › Letter › peer-review

18 Citations (Scopus)

Abstract

Clin Genet 1993: 44: 50. © Munksgaard, 1993

Original language	English
Pages (from-to)	50
Number of pages	1
Journal	Clinical Genetics
Volume	44
Issue number	1
DOIs	https://doi.org/10.1111/j.1399-0004.1993.tb03843.x
Publication status	Published - 1993 Jul
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1111/j.1399-0004.1993.tb03843.x

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title = "The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization",

abstract = "Clin Genet 1993: 44: 50. {\textcopyright} Munksgaard, 1993",

author = "Yoshimitsu Fukushima and Tomonobu Hasegawa",

year = "1993",

month = jul,

doi = "10.1111/j.1399-0004.1993.tb03843.x",

language = "English",

volume = "44",

pages = "50",

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AU - Hasegawa, Tomonobu

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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

Abstract

ASJC Scopus subject areas

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