4.5 Letter

Homozygous truncation of SIX6 causes complex microphthalmia in humans

Related references

Note: Only part of the references are listed.
Letter Genetics & Heredity

Analysis of the developmental SIX6 homeobox gene in patients with anophthalmia/microphthalmia

ME Gallardo et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2004)

Article Ophthalmology

Absence of SIX6 mutations in microphthalmia, anophthalmia, and coloboma

S Aijaz et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2004)

Article Genetics & Heredity

14q(22) deletion in a familial case of anophthalmia with polydactyly

ME Ahmad et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2003)

Article Developmental Biology

Six3 and Six6 activity is modulated by members of the groucho family

J Lopez-Rios et al.

DEVELOPMENT (2003)