Verloes, A <br/><br/>
Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.  [electronic resource] 

 -  Journal of medical genetics  May 1991 
 - 297-303 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Multicenter Study; Review 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.28.5.297  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--classification<br/>Chromosomes, Human, Pair 13<br/>Consanguinity<br/>Diagnosis, Differential<br/>Female<br/>Fetal Death--etiology<br/>Fetal Diseases--diagnosis<br/>Fingers--abnormalities<br/>Genes, Recessive<br/>Holoprosencephaly--classification<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Prenatal Diagnosis<br/>Syndrome<br/>Thanatophoric Dysplasia--diagnosis<br/>Trisomy