144 related articles for article (PubMed ID: 36094357)
1. Two siblings with GAPO syndrome: a novel missense variant in ANTXR1.
Yildiz O; Taşdelen E; Karakaya T; Taşdelen H
Clin Dysmorphol; 2022 Oct; 31(4):191-195. PubMed ID: 36094357
[No Abstract] [Full Text] [Related]
2. Dental Management of Siblings with GAPO Syndrome.
Kim A; Rogers S; Archibald J; Chandwani N
J Dent Child (Chic); 2021 May; 88(2):134-139. PubMed ID: 34321146
[TBL] [Abstract][Full Text] [Related]
3. Prenatal onset GAPO syndrome with a novel ANTXR1 variant in an Indian child: Expansion of the phenotype & literature review.
Balakrishnan S; Goud I; Teegala ML
Eur J Med Genet; 2024 Apr; 68():104929. PubMed ID: 38423276
[TBL] [Abstract][Full Text] [Related]
4. Distribution of
Gupta V; Panigrahi A; Somarajan BI; Gupta S; Tripathy K; Singh A; Sharma A; Tandon R; Pradhan D; Sharma A; Kushwaha T; Inampudi KK
Mol Vis; 2023; 29():365-377. PubMed ID: 38577561
[TBL] [Abstract][Full Text] [Related]
5. A novel mutation at ANTXR1 in an Indian patient with growth retardation-alopecia-pseudoanodontia-optic atrophy syndrome.
Chattopadhyay E; Ghose S; Ray A; Anjum N; Mazumdar A; Roy B
Oral Surg Oral Med Oral Pathol Oral Radiol; 2017 Nov; 124(5):e261-e265. PubMed ID: 28870703
[TBL] [Abstract][Full Text] [Related]
6. Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome.
Bayram Y; Pehlivan D; Karaca E; Gambin T; Jhangiani SN; Erdin S; Gonzaga-Jauregui C; Wiszniewski W; Muzny D; ; Elcioglu NH; Yildirim MS; Bozkurt B; Zamani AG; Boerwinkle E; Gibbs RA; Lupski JR
Am J Med Genet A; 2014 Sep; 164A(9):2328-34. PubMed ID: 25045128
[TBL] [Abstract][Full Text] [Related]
7. GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.
Abdel-Hamid MS; Ismail S; Zaki MS; Abdel-Salam GMH; Otaify GA; Issa MY; Abdel-Kader M; Girgis M; Aboul-Ezz E; Mazen I; Aglan MS; Temtamy SA
Am J Med Genet A; 2019 Feb; 179(2):237-242. PubMed ID: 30575274
[TBL] [Abstract][Full Text] [Related]
8. ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.
Przyklenk M; Karmacharya S; Bonasera D; Pasanen-Zentz AL; Kmoch S; Paulsson M; Wagener R; Liccardi G; Schiavinato A
Sci Rep; 2024 Apr; 14(1):9321. PubMed ID: 38653789
[TBL] [Abstract][Full Text] [Related]
9. Changing facial features in a child with GAPO syndrome caused by novel mutation in the ANTXR1 gene and uniparental disomy of chromosome 2.
Smigiel R; Rozensztrauch A; Walczak A; Rydzanicz M; Stawinski P; Berghausen-Mazur M; Kostrzewa G; Sasiadek M; Ploski R
Clin Dysmorphol; 2019 Oct; 28(4):211-214. PubMed ID: 31425299
[No Abstract] [Full Text] [Related]
10. Mutations in ANTXR1 cause GAPO syndrome.
Stránecký V; Hoischen A; Hartmannová H; Zaki MS; Chaudhary A; Zudaire E; Nosková L; Barešová V; Přistoupilová A; Hodaňová K; Sovová J; Hůlková H; Piherová L; Hehir-Kwa JY; de Silva D; Senanayake MP; Farrag S; Zeman J; Martásek P; Baxová A; Afifi HH; St Croix B; Brunner HG; Temtamy S; Kmoch S
Am J Hum Genet; 2013 May; 92(5):792-9. PubMed ID: 23602711
[TBL] [Abstract][Full Text] [Related]
11. GAPO syndrome with deafness: new feature or incidental finding?
Aggarwal S; Uttarilli A; Dalal AB
Clin Dysmorphol; 2013 Oct; 22(4):161-163. PubMed ID: 24326960
[No Abstract] [Full Text] [Related]
12. Telogen hair loss and androgenetic-like alopecia in GAPO syndrome.
Ahmed B; Gritli S
Australas J Dermatol; 2019 May; 60(2):e142-e144. PubMed ID: 30255493
[TBL] [Abstract][Full Text] [Related]
13. GAPO syndrome: a new syndromic cause of premature ovarian insufficiency.
Benetti-Pinto CL; Ferreira V; Andrade L; Yela DA; De Mello MP
Climacteric; 2016 Dec; 19(6):594-598. PubMed ID: 27426988
[TBL] [Abstract][Full Text] [Related]
14. GAPO syndrome: a novel variant in ANTXR1 gene.
Damagatla M; Verma A; Pochaboina V; Bhate M; Senthil S
Ophthalmic Genet; 2024 May; ():1-6. PubMed ID: 38691016
[TBL] [Abstract][Full Text] [Related]
15. GAPO syndrome: a rare genodermatosis presenting with unique features.
Troxell TN; Piccinin MA; Smith CM; Parsons ME; Drew GS
Int J Dermatol; 2018 Jun; 57(6):727-728. PubMed ID: 29377094
[No Abstract] [Full Text] [Related]
16. Arterial and venous thrombosis of the cerebral vasculature in GAPO syndrome.
Zeydan B; Benbir G; Uluduz D; Ince B; Goksan B; Islak C
Am J Med Genet A; 2014 May; 164A(5):1284-8. PubMed ID: 24664815
[TBL] [Abstract][Full Text] [Related]
17. GAPO syndrome with the novel features of pulmonary hypertension, ankyloglossia, and prognathism.
Demirgüneş EF; Ersoy-Evans S; Karaduman A
Am J Med Genet A; 2009 Feb; 149A(4):802-5. PubMed ID: 19291762
[No Abstract] [Full Text] [Related]
18. GAPO syndrome with craniosynostosis and intracranial hypertension.
Golpayegani M; Salari F; Habibi Z; Naderian N; Nejat F
Childs Nerv Syst; 2019 Sep; 35(9):1621-1624. PubMed ID: 31230109
[TBL] [Abstract][Full Text] [Related]
19. Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection.
Chen PR; Rowland RRR; Stoian AM; Petrovan V; Sheahan M; Ganta C; Cino-Ozuna G; Kim DY; Dunleavey JM; Whitworth KM; Samuel MS; Spate LD; Cecil RF; Benne JA; Yan X; Fang Y; Croix BS; Lechtenberg K; Wells KD; Prather RS
Sci Rep; 2022 Mar; 12(1):5009. PubMed ID: 35322150
[TBL] [Abstract][Full Text] [Related]
20. GAPO syndrome associated with vestibular dysfunction and hearing loss.
Rapsomaniki M; Chiarella G; Mascaro I; Ceravolo F; Cassandro E; Strisciuglio P; Concolino D
Am J Med Genet A; 2013 Aug; 161A(8):2102-4. PubMed ID: 23794220
[No Abstract] [Full Text] [Related]
[Next] [New Search]
