APA

Wimplinger I., Rauch A., Orth U., Schwarzer U., Trautmann U. & Kutsche K. (20080311). Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome. : European journal of medical genetics.

Chicago

Wimplinger Isabella, Rauch Anita, Orth Ulrike, Schwarzer Ulrich, Trautmann Udo and Kutsche Kerstin. 20080311. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome. : European journal of medical genetics.

Harvard

Wimplinger I., Rauch A., Orth U., Schwarzer U., Trautmann U. and Kutsche K. (20080311). Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome. : European journal of medical genetics.

MLA

Wimplinger Isabella, Rauch Anita, Orth Ulrike, Schwarzer Ulrich, Trautmann Udo and Kutsche Kerstin. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome. : European journal of medical genetics. 20080311.