158 related articles for article (PubMed ID: 33993843)
1. Dinosaur Tail Appendix in Trisomy 13.
Boșoteanu M; Orășanu CI; Așchie M; Deacu M; Cozaru GC; Brînzan C; Mitroi AF
Fetal Pediatr Pathol; 2022 Aug; 41(4):698-700. PubMed ID: 33993843
[No Abstract] [Full Text] [Related]
2. Longevity and Patau syndrome: what determines survival?
Peroos S; Forsythe E; Pugh JH; Arthur-Farraj P; Hodes D
BMJ Case Rep; 2012 Dec; 2012():. PubMed ID: 23220825
[TBL] [Abstract][Full Text] [Related]
3. Trisomy 13 by robertsonian translocation rob (13;13)(q10;q10) +13: about one case.
Laudat A; Serero S; Seridi I; Burc-Struxiano L
Ann Biol Clin (Paris); 2017 Dec; 75(6):695-698. PubMed ID: 29043983
[TBL] [Abstract][Full Text] [Related]
4. Parent-reported histories of adults with trisomy 13 syndrome.
Lebedoff AN; Carey JC
Am J Med Genet A; 2021 Jun; 185(6):1743-1756. PubMed ID: 33750000
[TBL] [Abstract][Full Text] [Related]
5. Survival Outcomes of Infants with the Trisomy 13 or Trisomy 18 Syndromes.
Carey JC
J Pediatr; 2022 Aug; 247():11-13. PubMed ID: 35640673
[No Abstract] [Full Text] [Related]
6. Holoprosencephaly in Patau Syndrome.
Schlosser AS; Costa GJC; Silva HSD; Mello JLM; Gomes LO; Onoyama MMO; Costa TMC
Rev Paul Pediatr; 2023; 41():e2022027. PubMed ID: 36921175
[TBL] [Abstract][Full Text] [Related]
7. Overlap of Patau and Pierre Robin syndromes along with abnormal metabolism: an interesting case study.
Jaiswal SK; Sukla KK; Gupta V; Rai AK
J Genet; 2014 Dec; 93(3):865-8. PubMed ID: 25572249
[No Abstract] [Full Text] [Related]
8. Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature.
Douglas C; Smith SA; Rohena L
Am J Med Genet A; 2017 Jun; 173(6):1673-1680. PubMed ID: 28394407
[TBL] [Abstract][Full Text] [Related]
9. Primary congenital glaucoma associated with Patau syndrome with long survival.
Jaru-Ampornpan P; Kuchtey J; Dev VG; Kuchtey R
J Pediatr Ophthalmol Strabismus; 2010 Jun; 47 Online():e1-4. PubMed ID: 21080618
[TBL] [Abstract][Full Text] [Related]
10. An interesting coexistence of Patau syndrome; Spigelian hernia and undescended testes.
Demir N; Tuncer O; Peker E; Bilici S; Yavuz A
Genet Couns; 2014; 25(2):241-4. PubMed ID: 25059026
[No Abstract] [Full Text] [Related]
11. Autopsy report of a 7-year old patient with the mosaic trisomy 13.
Imataka G; Yamanouchi H; Hirato J; Eguchi M; Kojima M; Honma K; Arisaka O
Cell Biochem Biophys; 2013 Nov; 67(2):813-7. PubMed ID: 23526188
[TBL] [Abstract][Full Text] [Related]
12. Patau syndrome with long survival in a case of unusual mosaic trisomy 13.
Fogu G; Maserati E; Cambosu F; Moro MA; Poddie F; Soro G; Bandiera P; Serra G; Tusacciu G; Sanna G; Mazzarello V; Montella A
Eur J Med Genet; 2008; 51(4):303-14. PubMed ID: 18495567
[TBL] [Abstract][Full Text] [Related]
13. Identification of Chromosome 17 Trisomy in a Cynomolgus Monkey (Macaca fascicularis) by Multicolor FISH Techniques.
Kimura A; Yahashi S; Chatani F; Tanabe H
Cytogenet Genome Res; 2021; 161(5):243-248. PubMed ID: 34265761
[TBL] [Abstract][Full Text] [Related]
14. Extensive comedonal and cystic acne in Patau syndrome.
Torrelo A; Fernandez-Crehuet P; Del Prado E; Martes P; Hernández-Martín A; De Diego V; Carapeto F
Pediatr Dermatol; 2010; 27(2):199-200. PubMed ID: 20537076
[TBL] [Abstract][Full Text] [Related]
15. [CONSIDERATIONS ON A CASE OF THE TRISOMY 13-15 SYNDROME (PATAU SYNDROME)].
ANDREESCU F; MARINESCU M
Pediatria (Bucur); 1965; 14():39-43. PubMed ID: 14322226
[No Abstract] [Full Text] [Related]
16. A TRISOMY 13 CASE PRESENTING WITH CONGENITAL DIAPHRAGMATIC HERNIA AND MICROPHTHALMIA.
Sahin S; Kutman KH; Bozkurt O; Canpolat FE; Uras N; Oguz SS; Topcu V; Ozdemir O; Dilmen U
Genet Couns; 2015; 26(2):263-5. PubMed ID: 26349200
[No Abstract] [Full Text] [Related]
17. A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic Mechanism.
Monin P; Reynaud N; Hanna N; Dupuis-Girod S; Till M; Arnaud P; Labalme A; Alix E; Poizat-Amar C; Faoucher M; Ravella L; Debost B; Obadia JF; Zech JC; Boileau C; Sanlaville D; Edery P; Putoux A; Schluth-Bolard C
Cytogenet Genome Res; 2020; 160(2):72-79. PubMed ID: 32187601
[TBL] [Abstract][Full Text] [Related]
18. Hidradenitis suppurativa in patients with trisomy 13: a scoping review.
Mehta S; Metko D; Sibbald C
Arch Dermatol Res; 2024 Jun; 316(7):433. PubMed ID: 38935334
[No Abstract] [Full Text] [Related]
19. [Mosaic trisomy 13].
Cammarata-Scalisi F; Araque D; Lacruz-Rengel MA; Valera-Ruíz B
An Pediatr (Barc); 2013 Dec; 79(6):402-3. PubMed ID: 23684171
[No Abstract] [Full Text] [Related]
20. A girl with metopic synostosis and trisomy 13 mosaicism: case report and review of the literature.
Aypar E; Yildirim MS; Sert A; Ciftci I; Odabas D
Am J Med Genet A; 2011 Mar; 155A(3):638-41. PubMed ID: 21344634
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
