APA

Gould D. B., Jaafar M. S., Addison M. K., Munier F., Ritch R., MacDonald I. M. & Walter M. A. (20040729). Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment. : BMC medical genetics.

Chicago

Gould Douglas B, Jaafar Mohamad S, Addison Mark K, Munier Francis, Ritch Robert, MacDonald Ian M and Walter Michael A. 20040729. Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment. : BMC medical genetics.

Harvard

Gould D. B., Jaafar M. S., Addison M. K., Munier F., Ritch R., MacDonald I. M. and Walter M. A. (20040729). Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment. : BMC medical genetics.

MLA

Gould Douglas B, Jaafar Mohamad S, Addison Mark K, Munier Francis, Ritch Robert, MacDonald Ian M and Walter Michael A. Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment. : BMC medical genetics. 20040729.