172 related articles for article (PubMed ID: 23763483)
21. The ATPase SRCAP is associated with the mitotic apparatus, uncovering novel molecular aspects of Floating-Harbor syndrome.
Messina G; Prozzillo Y; Delle Monache F; Santopietro MV; Atterrato MT; Dimitri P
BMC Biol; 2021 Sep; 19(1):184. PubMed ID: 34474679
[TBL] [Abstract][Full Text] [Related]
22. Renal Calculus in Floating-Harbor Syndrome: A Case Report.
Shields LBE; Peppas DS; Rosenberg E
J Pediatr Health Care; 2019 Jan; 33(1):97-101. PubMed ID: 30205917
[TBL] [Abstract][Full Text] [Related]
23. Case Report of Floating-Harbor Syndrome With Bilateral Cleft Lip.
Ko J; Pomerantz JH; Perry H; Shieh JT; Slavotinek AM; Oberoi S; Klein OD
Cleft Palate Craniofac J; 2020 Jan; 57(1):132-136. PubMed ID: 31248274
[TBL] [Abstract][Full Text] [Related]
24. [Floating-Harbor syndrome: a case report and literature review].
Li RM; Lu YC; Li Z; Wang JY; Chang J; Lei SQ; Zeng Q; Sang YM
Zhongguo Dang Dai Er Ke Za Zhi; 2019 Dec; 21(12):1208-1211. PubMed ID: 31874661
[TBL] [Abstract][Full Text] [Related]
25. Clinical and genetic characteristics and effects of long-term growth hormone therapy in a girl with Floating-Harbor syndrome.
García RJ; Kant SG; Wit JM; Mericq V
J Pediatr Endocrinol Metab; 2012; 25(1-2):207-12. PubMed ID: 22570979
[TBL] [Abstract][Full Text] [Related]
26. Floating Harbor syndrome. Case report and further syndrome delineation.
Midro AT; Olchowik B; Rogowska M; Hubert E; Hassman-Poznańska E; Papasz A; Szulc S; Wiśniewski A
Ann Genet; 1997; 40(3):133-8. PubMed ID: 9401100
[TBL] [Abstract][Full Text] [Related]
27. Changing phenotype in Floating-Harbor syndrome.
Hersh JH; Groom KR; Yen FF; Verdi GD
Am J Med Genet; 1998 Feb; 76(1):58-61. PubMed ID: 9508066
[TBL] [Abstract][Full Text] [Related]
28. Search for a gene responsible for Floating-Harbor syndrome on chromosome 12q15q21.1.
Lopez E; Callier P; Cormier-Daire V; Lacombe D; Moncla A; Bottani A; Lambert S; Goldenberg A; Doray B; Odent S; Sanlaville D; Gueneau L; Duplomb L; Huet F; Aral B; Thauvin-Robinet C; Faivre L
Am J Med Genet A; 2012 Feb; 158A(2):333-9. PubMed ID: 22247066
[TBL] [Abstract][Full Text] [Related]
29. Floating-Harbor syndrome with chorioretinal colobomas.
Alanis S; Blair MP; Kaufman LM; Bhat G; Shapiro MJ
Ophthalmic Genet; 2024 Apr; 45(2):207-209. PubMed ID: 37722826
[TBL] [Abstract][Full Text] [Related]
30. Intracranial vascular pathology in two further patients with Floating-Harbor syndrome: Proposals for cerebrovascular disease risk management.
Menzies L; D'Arco F; Ganesan V; Hurst JA
Eur J Med Genet; 2020 Apr; 63(4):103785. PubMed ID: 31605816
[TBL] [Abstract][Full Text] [Related]
31. Anaesthesia for open-heart surgery in a patient with Weaver's syndrome.
Celebioglu B; Yener F
Eur J Anaesthesiol; 2002 Dec; 19(12):897-8. PubMed ID: 12510911
[No Abstract] [Full Text] [Related]
32. [4p deletion syndrome].
Narahara K
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):309-11. PubMed ID: 11057240
[No Abstract] [Full Text] [Related]
33. Generation of an induced pluripotent stem cell line from a Chinese Han infant with floating-harbor syndrome accompanied with dilated cardiomyopathy.
Hou C; Xie L; Qiu Q; Lin H; Liu W; Sun X; Zhang Y; Xu M; Li Y; Xiao T
Stem Cell Res; 2021 Mar; 51():102182. PubMed ID: 33517121
[TBL] [Abstract][Full Text] [Related]
34. Baraitser-Winter cerebrofrontofacial syndrome.
Yates TM; Turner CL; Firth HV; Berg J; Pilz DT
Clin Genet; 2017 Jul; 92(1):3-9. PubMed ID: 27625340
[TBL] [Abstract][Full Text] [Related]
35. Stratton-Parker syndrome: confirmation of a new entity.
Gabrielli O; Carloni I; Catassi C; Natalini G; Coppa GV; Giorgi P
Am J Med Genet; 1994 Feb; 49(3):333-6. PubMed ID: 8209896
[TBL] [Abstract][Full Text] [Related]
36. Floating Harbor Syndrome.
Amita M; Srivastava P; Agarwal D; Phadke SR
Indian J Pediatr; 2016 Aug; 83(8):896-7. PubMed ID: 27206688
[No Abstract] [Full Text] [Related]
37. Pachygyria in Weaver syndrome.
Freeman BM; Hoon AH; Breiter SN; Hamosh A
Am J Med Genet; 1999 Oct; 86(4):395-7. PubMed ID: 10494098
[No Abstract] [Full Text] [Related]
38. Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome.
Tong TM; Hau EW; Lo IF; Chan DH; Lam ST
Chin Med J (Engl); 2005 Sep; 118(18):1499-506. PubMed ID: 16232326
[TBL] [Abstract][Full Text] [Related]
39. Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.
Aramaki M; Udaka T; Kosaki R; Makita Y; Okamoto N; Yoshihashi H; Oki H; Nanao K; Moriyama N; Oku S; Hasegawa T; Takahashi T; Fukushima Y; Kawame H; Kosaki K
J Pediatr; 2006 Mar; 148(3):410-4. PubMed ID: 16615981
[TBL] [Abstract][Full Text] [Related]
40. Floating-Harbor syndrome in two sisters: autosomal recessive inheritance or germinal mosaicism?
Ioan DM; Fryns JP
Genet Couns; 2003; 14(4):431-3. PubMed ID: 14738118
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
