Original language | English |
---|---|
Pages (from-to) | 50 |
Number of pages | 1 |
Journal | Clinical Genetics |
Volume | 44 |
Issue number | 1 |
Publication status | Published - 1993 |
Externally published | Yes |
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ASJC Scopus subject areas
- Genetics
- Genetics(clinical)
Cite this
The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization [3]. / Fukushima, Y.; Hasegawa, Tomonobu; Hasegawa, T.
In: Clinical Genetics, Vol. 44, No. 1, 1993, p. 50.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization [3]
AU - Fukushima, Y.
AU - Hasegawa, Tomonobu
AU - Hasegawa, T.
PY - 1993
Y1 - 1993
UR - http://www.scopus.com/inward/record.url?scp=0027199727&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027199727&partnerID=8YFLogxK
M3 - Article
C2 - 8403456
AN - SCOPUS:0027199727
VL - 44
SP - 50
JO - Clinical Genetics
JF - Clinical Genetics
SN - 0009-9163
IS - 1
ER -