Laurent, C <br/><br/>
[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].  [electronic resource] 

 -  Humangenetik  1973 
 - 321-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0018-7348 
<br/><br/><label>Standard No.: </label>10.1007/BF00291129  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosomes, Human, 6-12 and X<br/>Eye Abnormalities<br/>Female<br/>Growth Disorders--genetics<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Infant<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Micrognathism--genetics<br/>Palate--abnormalities<br/>Pedigree<br/>Trisomy