207 related articles for article (PubMed ID: 24123833)
1. Developmental disease and cancer: biological and clinical overlaps.
Bellacosa A
Am J Med Genet A; 2013 Nov; 161A(11):2788-96. PubMed ID: 24123833
[TBL] [Abstract][Full Text] [Related]
2. Developmental disorders with intellectual disability driven by chromatin dysregulation: Clinical overlaps and molecular mechanisms.
Larizza L; Finelli P
Clin Genet; 2019 Feb; 95(2):231-240. PubMed ID: 29672823
[TBL] [Abstract][Full Text] [Related]
3. Ocular manifestations of genetic and developmental diseases.
Hertle RW
Curr Opin Ophthalmol; 1997 Dec; 8(6):66-73. PubMed ID: 10176106
[TBL] [Abstract][Full Text] [Related]
4. Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.
Tatton-Brown K; Loveday C; Yost S; Clarke M; Ramsay E; Zachariou A; Elliott A; Wylie H; Ardissone A; Rittinger O; Stewart F; Temple IK; Cole T; ; Mahamdallie S; Seal S; Ruark E; Rahman N
Am J Hum Genet; 2017 May; 100(5):725-736. PubMed ID: 28475857
[TBL] [Abstract][Full Text] [Related]
5. Developmental defects and childhood cancer.
Slavin TP; Wiesner GL
Curr Opin Pediatr; 2009 Dec; 21(6):717-23. PubMed ID: 19812499
[TBL] [Abstract][Full Text] [Related]
6. Developmental Delay and Colon Polyposis.
Samadder NJ; Burt RW; Toydemir RM
Gastroenterology; 2017 Oct; 153(4):908-909. PubMed ID: 28881184
[No Abstract] [Full Text] [Related]
7. Microdeletions in 16p11.2 and 13q31.3 associated with developmental delay and generalized overgrowth.
George AM; Taylor J; Love DR
Genet Mol Res; 2012 Sep; 11(3):3133-7. PubMed ID: 23007991
[TBL] [Abstract][Full Text] [Related]
8. A case of autism in a child with Apert's syndrome.
Morey-Canellas J; Sivagamasundari U; Barton H
Eur Child Adolesc Psychiatry; 2003 Apr; 12(2):100-2. PubMed ID: 12664274
[TBL] [Abstract][Full Text] [Related]
9. A new missense mutation in DPF2 gene related to Coffin Siris syndrome 7: Description of a mild phenotype expanding DPF2-related clinical spectrum and differential diagnosis among similar syndromes epigenetically determined.
Milone R; Gnazzo M; Stefanutti E; Serafin D; Novelli A
Brain Dev; 2020 Feb; 42(2):192-198. PubMed ID: 31706665
[TBL] [Abstract][Full Text] [Related]
10. Hereditary cancer predisposition syndromes.
Garber JE; Offit K
J Clin Oncol; 2005 Jan; 23(2):276-92. PubMed ID: 15637391
[TBL] [Abstract][Full Text] [Related]
11. Developmental disabilities: genetic implications.
Ross LJ
J Obstet Gynecol Neonatal Nurs; 1994; 23(6):502-5. PubMed ID: 7525904
[TBL] [Abstract][Full Text] [Related]
12. Regarding cancer predisposition detected by CHG arrays.
Collins DL; Schimke RN
Genet Med; 2011 Nov; 13(11):982; author reply 982-3. PubMed ID: 22051689
[No Abstract] [Full Text] [Related]
13. Research progress of epigenetic biomarkers in the early diagnosis and treatment of human diseases.
Li W; Qin J; Wang H; Chen LB
Yi Chuan; 2018 Feb; 40(2):104-115. PubMed ID: 29428903
[TBL] [Abstract][Full Text] [Related]
14. Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
Machol K; Rousseau J; Ehresmann S; Garcia T; Nguyen TTM; Spillmann RC; Sullivan JA; Shashi V; Jiang YH; Stong N; Fiala E; Willing M; Pfundt R; Kleefstra T; Cho MT; McLaughlin H; Rosello Piera M; Orellana C; Martínez F; Caro-Llopis A; Monfort S; Roscioli T; Nixon CY; Buckley MF; Turner A; Jones WD; van Hasselt PM; Hofstede FC; van Gassen KLI; Brooks AS; van Slegtenhorst MA; Lachlan K; Sebastian J; Madan-Khetarpal S; Sonal D; Sakkubai N; Thevenon J; Faivre L; Maurel A; Petrovski S; Krantz ID; Tarpinian JM; Rosenfeld JA; Lee BH; ; Campeau PM
Am J Hum Genet; 2019 Jan; 104(1):164-178. PubMed ID: 30580808
[TBL] [Abstract][Full Text] [Related]
15. Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?
Stradella A; Del Valle J; Rofes P; Feliubadaló L; Grau Garces È; Velasco À; González S; Vargas G; Izquierdo Á; Campos O; Tornero E; Navarro M; Balmaña-Gelpi J; Capellá G; Pineda M; Brunet J; Lázaro C
J Med Genet; 2019 Aug; 56(8):521-525. PubMed ID: 30580288
[TBL] [Abstract][Full Text] [Related]
16. The Deciphering Developmental Disorders (DDD) study.
Firth HV; Wright CF;
Dev Med Child Neurol; 2011 Aug; 53(8):702-3. PubMed ID: 21679367
[No Abstract] [Full Text] [Related]
17. Bone marrow transplantation for Nijmegan breakage syndrome.
Gennery AR; Slatter MA; Bhattacharya A; Jeggo PA; Abinun M; Flood TJ; Cant AJ
J Pediatr Hematol Oncol; 2005 Apr; 27(4):239. PubMed ID: 15838402
[No Abstract] [Full Text] [Related]
18. Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.
Moreno-De-Luca A; Myers SM; Challman TD; Moreno-De-Luca D; Evans DW; Ledbetter DH
Lancet Neurol; 2013 Apr; 12(4):406-14. PubMed ID: 23518333
[TBL] [Abstract][Full Text] [Related]
19. Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.
Ripperger T; Bielack SS; Borkhardt A; Brecht IB; Burkhardt B; Calaminus G; Debatin KM; Deubzer H; Dirksen U; Eckert C; Eggert A; Erlacher M; Fleischhack G; Frühwald MC; Gnekow A; Goehring G; Graf N; Hanenberg H; Hauer J; Hero B; Hettmer S; von Hoff K; Horstmann M; Hoyer J; Illig T; Kaatsch P; Kappler R; Kerl K; Klingebiel T; Kontny U; Kordes U; Körholz D; Koscielniak E; Kramm CM; Kuhlen M; Kulozik AE; Lamottke B; Leuschner I; Lohmann DR; Meinhardt A; Metzler M; Meyer LH; Moser O; Nathrath M; Niemeyer CM; Nustede R; Pajtler KW; Paret C; Rasche M; Reinhardt D; Rieß O; Russo A; Rutkowski S; Schlegelberger B; Schneider D; Schneppenheim R; Schrappe M; Schroeder C; von Schweinitz D; Simon T; Sparber-Sauer M; Spix C; Stanulla M; Steinemann D; Strahm B; Temming P; Thomay K; von Bueren AO; Vorwerk P; Witt O; Wlodarski M; Wössmann W; Zenker M; Zimmermann S; Pfister SM; Kratz CP
Am J Med Genet A; 2017 Apr; 173(4):1017-1037. PubMed ID: 28168833
[TBL] [Abstract][Full Text] [Related]
20. Confirmation and further delineation of the SMG9-deficiency syndrome, a rare and severe developmental disorder.
Lecoquierre F; Bonnevalle A; Chadie A; Gayet C; Dumant-Forest C; Renaux-Petel M; Leca JB; Hazelzet T; Brasseur-Daudruy M; Louillet F; Muraine M; Coutant S; Quenez O; Boland A; Deleuze JF; Frebourg T; Goldenberg A; Saugier-Veber P; Guerrot AM; Nicolas G
Am J Med Genet A; 2019 Nov; 179(11):2257-2262. PubMed ID: 31390136
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
