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Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern

✍ Scribed by T. Ogata; Keiko Wakui; Koji Muroya; Hirofumi Ohashi; Nobutake Matsuo; Donna M. Brown; Takashi Ishii; Yoshimitsu Fukushima


Publisher
Springer
Year
1998
Tongue
English
Weight
90 KB
Volume
103
Category
Article
ISSN
0340-6717

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