143 related articles for article (PubMed ID: 23396887)
1. [Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?].
Shongo MY; Lubala TK; Mbuyi SM; Makinko PI; Ngwej DT; Kabange FN
Pan Afr Med J; 2012; 13():85. PubMed ID: 23396887
[TBL] [Abstract][Full Text] [Related]
2. De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2.
Tassano E; Di Rocco M; Signa S; Gimelli G
Am J Med Genet A; 2013 Apr; 161A(4):894-6. PubMed ID: 23495052
[No Abstract] [Full Text] [Related]
3. Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2.
Fiori E; Babicola L; Andolina D; Coassin A; Pascucci T; Patella L; Han YC; Ventura A; Ventura R
Behav Genet; 2015 Sep; 45(5):547-59. PubMed ID: 26026879
[TBL] [Abstract][Full Text] [Related]
4. GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION.
Atik T; Güvenç MS; Onay H; Özkinay F; Çoğulu Ö
Genet Couns; 2016; 27(3):381-384. PubMed ID: 30204967
[TBL] [Abstract][Full Text] [Related]
5. Metacarpophalangeal pattern profile analysis for a 3-month-old infant with Feingold syndrome 2.
Isobe A; Maeda N; Fujita H; Banno S; Kageyama T; Hatabu N; Sato R; Suzuki E; Miharu M; Komiyama O; Nakashima M; Matsunaga T; Nishimura G; Yamazawa K
Am J Med Genet A; 2021 Mar; 185(3):952-954. PubMed ID: 33369046
[No Abstract] [Full Text] [Related]
6. Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2.
Muriello M; Kim AY; Sondergaard Schatz K; Beck N; Gunay-Aygun M; Hoover-Fong JE
Am J Med Genet A; 2019 Mar; 179(3):410-416. PubMed ID: 30672094
[TBL] [Abstract][Full Text] [Related]
7. A fourth case of Feingold syndrome type 2: psychiatric presentation and management.
Ganjavi H; Siu VM; Speevak M; MacDonald PA
BMJ Case Rep; 2014 Nov; 2014():. PubMed ID: 25391829
[TBL] [Abstract][Full Text] [Related]
8. Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN.
Burnside RD; Molinari S; Botti C; Brooks SS; Chung WK; Mehta L; Schwartz S; Papenhausen P
Am J Med Genet A; 2018 Sep; 176(9):1956-1963. PubMed ID: 30088856
[TBL] [Abstract][Full Text] [Related]
9. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
Ravel A; Chouery E; Stora S; Jalkh N; Villard L; Temtamy S; Mégarbané A
Am J Med Genet A; 2011 Apr; 155A(4):880-4. PubMed ID: 21416592
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1.
Peleg A; Kurolap A; Sagi-Dain L; Larom-Khan G; Adir V; Mory A; Paperna T; Shuldiner AR; Gonzaga-Jauregui C; Adir N; Baris Feldman H; Wollstein R
Clin Dysmorphol; 2021 Apr; 30(2):71-75. PubMed ID: 32925198
[TBL] [Abstract][Full Text] [Related]
11. Feingold syndrome type 2 in a patient from China.
Lei J; Han L; Huang Y; Long M; Zhao G; Yan S; Zhang J
Am J Med Genet A; 2021 Jul; 185(7):2262-2266. PubMed ID: 33818875
[TBL] [Abstract][Full Text] [Related]
12. Adams-Oliver syndrome associated with gastrointestinal malformations.
van Geyzel L; Gribbon C; Bradley S; Duffy D
BMJ Case Rep; 2016 Nov; 2016():. PubMed ID: 27888223
[No Abstract] [Full Text] [Related]
13. A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.
Chen CP; Lin SP; Chern SR; Wu PS; Chang SD; Ng SH; Liu YP; Su JW; Wang W
Eur J Med Genet; 2012 Nov; 55(11):666-9. PubMed ID: 22842076
[TBL] [Abstract][Full Text] [Related]
14. Feingold syndome: a rare but important cause of syndromic tracheoesophageal fistula.
Layman-Pleet L; Jackson CC; Chou S; Boycott KM
J Pediatr Surg; 2007 Sep; 42(9):E1-3. PubMed ID: 17848225
[TBL] [Abstract][Full Text] [Related]
15. Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.
Cognet M; Nougayrede A; Malan V; Callier P; Cretolle C; Faivre L; Genevieve D; Goldenberg A; Heron D; Mercier S; Philip N; Sigaudy S; Verloes A; Sarnacki S; Munnich A; Vekemans M; Lyonnet S; Etchevers H; Amiel J; de Pontual L
Eur J Hum Genet; 2011 May; 19(5):602-6. PubMed ID: 21224895
[TBL] [Abstract][Full Text] [Related]
16. Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
Tedesco MG; Lonardo F; Ceccarini C; Cesarano C; Digilio MC; Magliozzi M; Rogaia D; Mencarelli A; Leoni C; Piscopo C; Imperatore V; Falco MT; Fontana P; Nardone AM; Novelli A; Troiani S; Seri M; Prontera P
Am J Med Genet A; 2021 Apr; 185(4):1204-1210. PubMed ID: 33442900
[TBL] [Abstract][Full Text] [Related]
17. Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association.
Hernández-García A; Brosens E; Zaveri HP; de Jong EM; Yu Z; Namwanje M; Mayle A; Fernandes CJ; Lee B; Blazo M; Lalani SR; Tibboel D; de Klein A; Scott DA
Am J Med Genet A; 2012 Jul; 158A(7):1785-7. PubMed ID: 22639458
[No Abstract] [Full Text] [Related]
18. The DATE Association: A Separate Entity or a Further Extension of the VACTERL Association?
Ceccanti S; Midrio P; Messina M; Mattioli G; Appignani A; Briganti V; Cheli M; Lima M; Cozzi DA
J Surg Res; 2019 Sep; 241():128-134. PubMed ID: 31022678
[TBL] [Abstract][Full Text] [Related]
19. Esophageal atresia and tracheoesophageal fistula malformations.
Ashcraft KW; Holder TM
Surg Clin North Am; 1976 Apr; 56(2):299-315. PubMed ID: 1265597
[No Abstract] [Full Text] [Related]
20. Esophageal atresia and tracheoesophageal fistula.
Saab SB; James E
Ear Nose Throat J; 1979 Nov; 58(11):494-9. PubMed ID: 544256
[No Abstract] [Full Text] [Related]
[Next] [New Search]
