- Belmont, John W.; Ware,
Stephanie M. (2005-10-26). "Genetics of
human heterotaxias".
European Journal of
Human Genetics. 14 (1): 17–25. doi:10.1038/sj.ejhg...
-
familial external ophthalmoplegia Visceral steatosis Viscero-atrial
heterotaxia Visna Maedi complex Vitamin A
embryopathy Vitamin B6
deficiency Vitamin...
- 14–16. PMID 18264930.[permanent dead link]
Brueckner M (June 2007). "
Heterotaxia,
congenital heart disease, and
primary ciliary dyskinesia". Circulation...
- Hers'
disease Hersh–Podruch–Weisskopk
syndrome Heterophobia Heterotaxia (generic term)
Heterotaxia autosomal dominant type
Heterotaxy with
polysplenia or asplenia...
-
organs Situs inversus, the
inverted disposition of
organs Situs ambiguus (
heterotaxia),
comprises mixed cases where only some
organs are
inverted Situ (office)...
-
isomerization of the lungs,
malformation of the
cardiac outflow tract,
heterotaxia, and/or
situs inversus. The
UniProt Consortium; UniProt: the universal...
- Van de Ven W,
Devriendt K (Apr 2003). "PA26 is a
candidate gene for
heterotaxia in humans:
identification of a
novel PA26-related gene
family in human...
- Hallermann–Streiff syndrome; and
heart malformations, such as viscero-atrial
heterotaxia.
There have also been a few
cases of
reported hearing loss and skin disorders...
- Van de Ven W,
Devriendt K (May 2003). "PA26 is a
candidate gene for
heterotaxia in humans:
identification of a
novel PA26-related gene
family in human...
- Pcsk6
knockout studies found that mice
embryos that lack Pcsk6
develop heterotaxia, left
pulmonary isomerism, and/or
craniofacial malformations due to disruption...
