Wauters, J G <br/><br/>
Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion.  [electronic resource] 

 -  Clinical genetics  Nov 1993 
 - 262-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.1993.tb03894.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Abortion, Therapeutic<br/>Chromosome Aberrations--diagnosis<br/>Chromosome Disorders<br/>Chromosome Inversion<br/>Chromosomes, Human, Pair 6<br/>Facial Bones--abnormalities<br/>Female<br/>Fetal Diseases--diagnosis<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant, Newborn<br/>Intellectual Disability--genetics<br/>Kidney--abnormalities<br/>Male<br/>Monosomy<br/>Mosaicism<br/>Pedigree<br/>Pregnancy<br/>Pregnancy Trimester, First<br/>Pregnancy Trimester, Second<br/>Pregnancy in Diabetics<br/>Prenatal Diagnosis<br/>Skull--abnormalities<br/>Trisomy