Orstavik, K H <br/><br/>
Severe craniofacial malformations and deglutition dysfunction in a brother and sister: new syndrome?  [electronic resource] 

 -  American journal of medical genetics  Jul 1998 
 - 260-2 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1096-8628(19980707)78:3<260::aid-ajmg10>3.0.co;2-d  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--classification<br/>Birth Weight<br/>Cleft Palate--genetics<br/>Craniofacial Abnormalities--classification<br/>Deglutition Disorders--classification<br/>Fatal Outcome<br/>Female<br/>Gastroesophageal Reflux<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Mosaicism<br/>Nuclear Family<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>Psychomotor Performance<br/>Radiography<br/>Receptor Protein-Tyrosine Kinases--genetics<br/>Receptor, Fibroblast Growth Factor, Type 2<br/>Receptors, Fibroblast Growth Factor--genetics<br/>Spinal Curvatures--genetics<br/>Syndrome