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Heterozygous deletion at 14q22.1–q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly

✍ Scribed by Shin Hayashi; Nobuhiko Okamoto; Yoshio Makita; Akira Hata; Issei Imoto; Johji Inazawa


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
171 KB
Volume
146A
Category
Article
ISSN
1552-4825

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