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Page 1
Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.
Kozma K, Bembea M, Jurca CM, Ioana M, Streață I, Şoşoi SŞ, Pirvu A, Petchesi CD, Szilágyi A, Sava CN, Jurca A, Ujfalusi A, Szűcs Z, Szakszon K. Kozma K, et al. Genes (Basel). 2021 Oct 23;12(11):1674. doi: 10.3390/genes12111674. Genes (Basel). 2021. PMID: 34828280 Free PMC article. Review.
Greig cephalopolysyndactyly syndrome (GCPS) is a rare genetic disorder (about 200 cases reported), characterized by macrocephaly, hypertelorism, and polysyndactyly. ...
Greig cephalopolysyndactyly syndrome (GCPS) is a rare genetic disorder (about 200 cases reported), characterized by mac
The Greig cephalopolysyndactyly syndrome.
Biesecker LG. Biesecker LG. Orphanet J Rare Dis. 2008 Apr 24;3:10. doi: 10.1186/1750-1172-3-10. Orphanet J Rare Dis. 2008. PMID: 18435847 Free PMC article. Review.
The Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome. ...
The Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome. ...
Hedgehog signaling update.
Cohen MM Jr. Cohen MM Jr. Am J Med Genet A. 2010 Aug;152A(8):1875-914. doi: 10.1002/ajmg.a.32909. Am J Med Genet A. 2010. PMID: 20635334 Review.
Disorders associated with the hedgehog signaling network follow, including nevoid basal cell carcinoma syndrome, holoprosencephaly, Smith-Lemli-Opitz syndrome, Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, Carpenter syndrome, and Rubinstein-T …
Disorders associated with the hedgehog signaling network follow, including nevoid basal cell carcinoma syndrome, holoprosencephaly, Smith-Le …
The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
Gollop TR, Fontes LR. Gollop TR, et al. Am J Med Genet. 1985 Sep;22(1):59-68. doi: 10.1002/ajmg.1320220106. Am J Med Genet. 1985. PMID: 3901752 Review.
The Greig cephalopolysyndactyly syndrome in characterized by a set of craniofacial defects (macrocephaly, broad nasal root) leading to peculiar facial appearance, postaxial (occasionally preaxial) polydactyly of hands, preaxial (rarely postaxial) polydactyly …
The Greig cephalopolysyndactyly syndrome in characterized by a set of craniofacial defects (macrocephaly, broad nasal r …
Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literature.
Ausems MG, Ippel PF, Renardel de Lavalette PA. Ausems MG, et al. Clin Dysmorphol. 1994 Jan;3(1):21-30. Clin Dysmorphol. 1994. PMID: 8205322 Review.
We report on a four generation family with Greig cephalopolysyndactyly syndrome. The clinical variability of the malformations of hands and feet is described. A review of the literature is given, with emphasis on the frequency of clinical signs of the Grei
We report on a four generation family with Greig cephalopolysyndactyly syndrome. The clinical variability of the malfor …
[Greig cephalopolysyndactyly syndrome].
Satokata I. Satokata I. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):184-6. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057189 Review. Japanese. No abstract available.
Birth defects caused by mutations in human GLI3 and mouse Gli3 genes.
Naruse I, Ueta E, Sumino Y, Ogawa M, Ishikiriyama S. Naruse I, et al. Congenit Anom (Kyoto). 2010 Mar;50(1):1-7. doi: 10.1111/j.1741-4520.2009.00266.x. Congenit Anom (Kyoto). 2010. PMID: 20201963 Review.
ABSTRACT GLI3 is the gene responsible for Greig cephalopolysyndactyly syndrome (GCPS), Pallister-Hall syndrome (PHS) and Postaxial polydactyly type-A (PAP-A). ...
ABSTRACT GLI3 is the gene responsible for Greig cephalopolysyndactyly syndrome (GCPS), Pallister-Hall syndrome (PHS) an …
Molecular genetic approaches to the study of human craniofacial dysmorphologies.
Moore GE. Moore GE. Int Rev Cytol. 1995;158:215-77. doi: 10.1016/s0074-7696(08)62488-2. Int Rev Cytol. 1995. PMID: 7721539 Review.
This article focuses on a subgroup of craniofacial dysmorphologies, covering these three main inheritance patterns, that are being studied using molecular biology techniques: DiGeorge syndrome, Treacher Collins syndrome, Greig cephalopolysyndactyly syndrome, …
This article focuses on a subgroup of craniofacial dysmorphologies, covering these three main inheritance patterns, that are being studied u …
[Sonic Hedgehog signaling pathway and regulation of inner ear development].
Chen ZQ, Han XH, Cao X. Chen ZQ, et al. Yi Chuan. 2013 Sep;35(9):1058-64. doi: 10.3724/sp.j.1005.2013.01058. Yi Chuan. 2013. PMID: 24400478 Review. Chinese.
In humans, diseases accompanied by hearing disorders caused by abnormal Shh signaling include Greig cephalopolysyndactyly syndrome (GCPS), Pallister-Hall syndrome (PHS), Waardenburg syndrome (WS) and medulloblastoma, etc. ...
In humans, diseases accompanied by hearing disorders caused by abnormal Shh signaling include Greig cephalopolysyndactyly s
Six cases of 7p deletion: clinical, cytogenetic, and molecular studies.
Chotai KA, Brueton LA, van Herwerden L, Garrett C, Hinkel GK, Schinzel A, Mueller RF, Speleman F, Winter RM. Chotai KA, et al. Am J Med Genet. 1994 Jul 1;51(3):270-6. doi: 10.1002/ajmg.1320510320. Am J Med Genet. 1994. PMID: 7521123 Review.
The putative proximal CRS locus at 7p13-->7p14 does not appear to be allelic with Greig cephalopolysyndactyly syndrome. Three probe positions have been refined: pJ5.11 (D7S10) previously mapped to 7p14-->pter does not appear to map proximal to p15; TM10 …
The putative proximal CRS locus at 7p13-->7p14 does not appear to be allelic with Greig cephalopolysyndactyly syndrome