118 related articles for article (PubMed ID: 26114601)
1. Additional patients with 4q deletion: Severe growth delay and polycystic kidney disease associated with 4q21q22 loss.
Sakazume S; Kido Y; Murakami N; Matsubara T; Numabe H
Pediatr Int; 2015 Oct; 57(5):880-3. PubMed ID: 26114601
[TBL] [Abstract][Full Text] [Related]
2. Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype.
Velinov M; Kupferman J; Gu H; Macera MJ; Babu A; Jenkins EC; Kupchik G
Eur J Med Genet; 2005; 48(1):51-5. PubMed ID: 15953406
[TBL] [Abstract][Full Text] [Related]
3. Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.
Hickey SE; Biswas S; Thrush DL; Pyatt RE; Gastier-Foster JM; Astbury C; Atkin J
Eur J Med Genet; 2013 Sep; 56(9):521-5. PubMed ID: 23895773
[TBL] [Abstract][Full Text] [Related]
4. Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy.
Sills ES; Burns MJ; Parker LD; Carroll LP; Kephart LL; Dyer CS; Papenhausen PR; Davis JG
Orphanet J Rare Dis; 2007 Feb; 2():9. PubMed ID: 17295911
[TBL] [Abstract][Full Text] [Related]
5. An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature review.
Vlaikou AM; Manolakos E; Noutsopoulos D; Markopoulos G; Liehr T; Vetro A; Ziegler M; Weise A; Kreskowski K; Papoulidis I; Thomaidis L; Syrrou M
Cytogenet Genome Res; 2014; 142(4):227-38. PubMed ID: 24733116
[TBL] [Abstract][Full Text] [Related]
6. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.
Bonnet C; Andrieux J; Béri-Dexheimer M; Leheup B; Boute O; Manouvrier S; Delobel B; Copin H; Receveur A; Mathieu M; Thiriez G; Le Caignec C; David A; de Blois MC; Malan V; Philippe A; Cormier-Daire V; Colleaux L; Flori E; Dollfus H; Pelletier V; Thauvin-Robinet C; Masurel-Paulet A; Faivre L; Tardieu M; Bahi-Buisson N; Callier P; Mugneret F; Edery P; Jonveaux P; Sanlaville D
J Med Genet; 2010 Jun; 47(6):377-84. PubMed ID: 20522426
[TBL] [Abstract][Full Text] [Related]
7. Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.
Kulharya AS; Maberry M; Kukolich MK; Day DW; Schneider NR; Wilson GN; Tonk V
Am J Med Genet; 1995 Jan; 55(2):165-70. PubMed ID: 7717415
[TBL] [Abstract][Full Text] [Related]
8. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
Rodovalho-Doriqui MJ; Freitas PL; Pinho JD; Cavalli LR; Pereira SR
Genet Mol Res; 2013 Jul; 12(3):2562-6. PubMed ID: 23979887
[TBL] [Abstract][Full Text] [Related]
9. Life-history chronicle for a patient with the recently described chromosome 4q21 microdeletion syndrome.
Tsang E; Rupps R; McGillivray B; Eydoux P; Marra M; Arbour L; Langlois S; Friedman JM; Zahir FR
Am J Med Genet A; 2012 Oct; 158A(10):2606-9. PubMed ID: 22903878
[TBL] [Abstract][Full Text] [Related]
10. Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.
Ronzoni L; Peron A; Bianchi V; Baccarin M; Guerneri S; Silipigni R; Lalatta F; Bedeschi MF
Am J Med Genet A; 2015 Jul; 167(7):1551-9. PubMed ID: 25851921
[TBL] [Abstract][Full Text] [Related]
11. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
12. The 4q-Syndrome.
Strehle EM; Ahmed OA; Hameed M; Russell A
Genet Couns; 2001; 12(4):327-39. PubMed ID: 11837601
[TBL] [Abstract][Full Text] [Related]
13. Subtelomeric Copy Number Variations: The Importance of 4p/4q Deletions in Patients with Congenital Anomalies and Developmental Disability.
Novo-Filho GM; Montenegro MM; Zanardo ÉA; Dutra RL; Dias AT; Piazzon FB; Costa TV; Nascimento AM; Honjo RS; Kim CA; Kulikowski LD
Cytogenet Genome Res; 2016; 149(4):241-246. PubMed ID: 27665090
[TBL] [Abstract][Full Text] [Related]
14. Investigation of 4q-deletion in two unrelated patients using array CGH.
Kaalund SS; Møller RS; Tészás A; Miranda M; Kosztolanyi G; Ullmann R; Tommerup N; Tümer Z
Am J Med Genet A; 2008 Sep; 146A(18):2431-4. PubMed ID: 18688872
[No Abstract] [Full Text] [Related]
15. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
[TBL] [Abstract][Full Text] [Related]
16. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
Nakane T; Kousuke N; Sonoko H; Yuko K; Sato H; Kubota T; Sugita K
Pediatr Int; 2013 Jun; 55(3):376-81. PubMed ID: 23782370
[TBL] [Abstract][Full Text] [Related]
17. De novo terminal 4q deletion syndrome with new ocular findings in Turkish twins: case report.
Sandal G; Ormeci AR; Oztas S
Genet Couns; 2013; 24(2):217-22. PubMed ID: 24032293
[TBL] [Abstract][Full Text] [Related]
18. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
[TBL] [Abstract][Full Text] [Related]
19. Familial tandem duplication of bands q31.1 to q32.3 on chromosome 4 with mild phenotypic effect.
Goodman BK; Capone GT; Hennessey J; Thomas GH
Am J Med Genet; 1997 Dec; 73(2):119-24. PubMed ID: 9409859
[TBL] [Abstract][Full Text] [Related]
20. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
