Weiss, L <br/><br/>
Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome.  [electronic resource] 

 -  American journal of diseases of children (1960)  Dec 1968 
 - 609-14 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0002-922X 
<br/><br/><label>Standard No.: </label>10.1001/archpedi.1968.02100020613007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Blood Group Antigens<br/>Child<br/>Chromosome Aberrations<br/>Chromosomes, Human, 13-15<br/>Chromosomes, Human, 21-22 and Y<br/>Chromosomes, Human, 6-12 and X<br/>Dermatoglyphics<br/>Down Syndrome--genetics<br/>Duodenal Obstruction--complications<br/>Female<br/>Heart Defects, Congenital--complications<br/>Humans<br/>Hyperbilirubinemia--complications<br/>Infant, Newborn<br/>Karyotyping<br/>Male<br/>Mitosis<br/>Mosaicism<br/>Pedigree<br/>Sex Chromosomes