- Nicolaides–
Baraitser syndrome (NCBRS) is a rare
genetic condition caused by de novo
missense mutations in the SMARCA2 gene and has only been reported...
- Temple–
Baraitser syndrome (TBS) is a very rare
autosomal dominant genetic disorder,
characterised by
intellectual disability, epilepsy,
small or absent...
- is now
reported to be
around 200. The
differential includes Nicolaides–
Baraitser syndrome. mild to
moderate to
severe intellectual disability, also called...
- Fryns-Aftimos
syndrome (also
known as
Baraitser-Winter
syndrome 1, or BWS1) is a rare
chromosomal condition and is ****ociated with pachygyria, severe...
- Bannayan–Zonana
syndrome Banti's
syndrome Bantu siderosis Baraitser–Brett–Piesowicz
syndrome Baraitser–Rodeck–Garner
syndrome Barber–Say
syndrome Barbiturate...
-
Baraitser was
appointed as the
presiding judge. On 21
October 2019, ****ange
appeared for a case
management hearing at the court. When
Judge Baraitser...
- 1038/ng1194-269. PMID 7874169. S2CID 40033932.
Rutland P;
Pulleyn LJ;
Reardon W;
Baraitser M;
Hayward R;
Jones B; et al. (1995). "Identical
mutations in the FGFR2...
- May 31, 2024.
Cameron ST,
Glasier A,
McDaid L,
Radley A,
Patterson S,
Baraitser P,
Stephenson J,
Gilson R,
Battison C,
Cowle K,
Vadiveloo T, Johnstone...
- (2): 122–32. doi:10.1017/S0012162200000232. PMID 10698330.
Patton MA,
Baraitser M,
Brett EM (February 1986). "A
family with
congenital suprabulbar paresis...
-
Intellectual developmental disorder 59 Saethre–Chotzen
syndrome Temple–
Baraitser syndrome Worth disease Artificial cranial deformation "Flat
forehead (Concept...
