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 - Concepedia

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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

58

Citations

21

References

2007

Year

Isabella Wimplinger, Anita Rauch, Ulrike Orth, Ulrich Schwarzer, Udo Trautmann, Kerstin Kutsche

European Journal of Medical Genetics

High Clinical VariabilityTerminal Xp DeletionGenetic DisorderLinear Skin DefectsPathologyDermatologyMedicine

References

	Year	Citations

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