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MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13
British Library Online Contents | 1999| -
Angelman Syndrome Due to Paternal Uniparental Disomy of Chromosome 15: A Milder Phenotype?
British Library Online Contents | 1994| -
High Incidence of Ectopic Nucleolar Organizer Regions in Human Testicular Tumors
British Library Online Contents | 1993| -
DNAI1 Mutations Explain Only 2% of Primary Ciliary Dykinesia
British Library Online Contents | 2008| -
Familial Translocation t(Y;15) (q12;p11) and De Novo Deletion of the Prader-Willi Syndrome (PWS) Critical Region on 15q11-q13
British Library Online Contents | 1997| -
Trisomy 3 mosaicism on CVS: case report with literature review and propositions for investigation and counseling
British Library Online Contents | 1995| -
Trisomy 12 Mosaicism Confirmed in Multiple Organs From a Liveborn Child
British Library Online Contents | 2000| -
Clinical significance of CVS mosaicism and non-mosaic fetoplacental discrepancies
British Library Conference Proceedings | 1997|
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