Made available in DSpace on 2022-04-29T08:40:16Z (GMT). No. of bitstreams: 0 Previous issue date: 2022-05-01; Holoprosencephaly is a central nervous system malformation, characterized by incomplete or total lack of division of prosencephalon hemispheres, which is commonly accompanied by craniofacial malformations. A 9-month-gestation aborted American Quarter Horse fetus was submitted for postmortem examination....
Made available in DSpace on 2022-05-01T15:13:39Z (GMT). No. of bitstreams: 0 Previous issue date: 2022-02-23; APAF1 is an autosomal recessive inherited mutation, associated with Holstein haplotype 1 (HH1) and characterized by a substitution of cytosine for a thymine (c.1741C>T) in chromosome 5. The mutation causes fetal and embryonic loss, between 60 and 200 days of gestation, and reduced conception rate. The A...