Weber, F M <br/><br/>
Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.  [electronic resource] 

 -  Cytogenetics  1971 
 - 404-12 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0011-4537 
<br/><br/><label>Standard No.: </label>10.1159/000130161  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Aneuploidy<br/>Autoradiography<br/>Blood Protein Electrophoresis<br/>Bone Marrow Cells<br/>Child, Preschool<br/>Chromosomes, Human, 21-22 and Y<br/>Female<br/>Fibroblasts--cytology<br/>Hair--cytology<br/>Humans<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Lymphocytes--cytology<br/>Microscopy, Fluorescence<br/>Mosaicism<br/>Mouth Mucosa--cytology<br/>Sex Chromatin<br/>Sex Chromosome Aberrations<br/>Thymidine--metabolism<br/>Tritium