Stoll, C <br/><br/>
Balanced familial translocation t(5;19)(q12;p or q11) with phenotypical abnormalities in a girl.  [electronic resource] 

 -  Humangenetik  1975 
 - 263-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0018-7348 
<br/><br/><label>Standard No.: </label>10.1007/BF00278357  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Carotid Arteries--abnormalities<br/>Child<br/>Chromosome Aberrations<br/>Chromosomes, Human, 19-20<br/>Chromosomes, Human, 4-5<br/>Chromosomes, Human, 6-12 and X<br/>Female<br/>Humans<br/>Karyotyping<br/>Phenotype<br/>Prognathism--genetics<br/>Translocation, Genetic<br/>Urinary Tract--abnormalities<br/>Vision Disorders--genetics