These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
188 related articles for article (PubMed ID: 7551160)
1. Microcephalic osteodysplastic primordial dwarfism type II. al Gazali LI; Hamada M; Lytle W Clin Dysmorphol; 1995 Jul; 4(3):234-8. PubMed ID: 7551160 [TBL] [Abstract][Full Text] [Related]
2. Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literature. Sigaudy S; Toutain A; Moncla A; Fredouille C; Bourlière B; Ayme S; Philip N Am J Med Genet; 1998 Oct; 80(1):16-24. PubMed ID: 9800907 [TBL] [Abstract][Full Text] [Related]
3. "Ocular moyamoya" syndrome in a patient with features of microcephalic osteodysplastic primordial dwarfism type II. Bang GM; Kirmani S; Patton A; Pulido JS; Brodsky MC J AAPOS; 2013 Feb; 17(1):100-2. PubMed ID: 23337351 [TBL] [Abstract][Full Text] [Related]
4. Microcephalic osteodysplastic primordial dwarfism type II: report of three cases and review. Majewski F; Goecke TO Am J Med Genet; 1998 Oct; 80(1):25-31. PubMed ID: 9800908 [TBL] [Abstract][Full Text] [Related]
5. Microcephalic osteodysplastic primordial dwarfism type I/III in sibs. Meinecke P; Passarge E J Med Genet; 1991 Nov; 28(11):795-800. PubMed ID: 1770539 [TBL] [Abstract][Full Text] [Related]
6. Osteodysplastic primordial dwarfism: report of a further case with manifestations similar to those of types I and III. Haan EA; Furness ME; Knowles S; Morris LL; Scott G; Svigos JM; Vigneswaren R Am J Med Genet; 1989 Jun; 33(2):224-7. PubMed ID: 2764032 [TBL] [Abstract][Full Text] [Related]
7. Neonatal cholestasis and focal medullary dysplasia of the kidneys in a case of microcephalic osteodysplastic primordial dwarfism. Berger A; Haschke N; Kohlhauser C; Amman G; Unterberger U; Weninger M J Med Genet; 1998 Jan; 35(1):61-4. PubMed ID: 9475098 [TBL] [Abstract][Full Text] [Related]
8. A 17-month-old with extreme prenatal-onset growth delay. Microcephalic osteodysplastic primordial dwarfism type II. Tekin M; Ng J; Bodurtha J Eur J Pediatr; 2000 Dec; 159(12):926-8. PubMed ID: 11131353 [No Abstract] [Full Text] [Related]
9. Re: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies [Kantaputra et al. 2004. Am J Med Genet 130A:181-190]. Hall JG Am J Med Genet A; 2005 May; 135(1):114; author reply 115. PubMed ID: 15723335 [No Abstract] [Full Text] [Related]
10. Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation. Abdel-Salam GMH; Sayed ISM; Afifi HH; Abdel-Ghafar SF; Abouzaid MR; Ismail SI; Aglan MS; Issa MY; El-Bassyouni HT; El-Kamah G; Effat LK; Eid M; Zaki MS; Temtamy SA; Abdel-Hamid MS Am J Med Genet A; 2020 Jun; 182(6):1407-1420. PubMed ID: 32267100 [TBL] [Abstract][Full Text] [Related]
11. Identification of three novel mutations in PCNT in vietnamese patients with microcephalic osteodysplastic primordial dwarfism type II. Nguyen TH; Nguyen NL; Vu CD; Ngoc CTB; Nguyen NK; Nguyen HH Genes Genomics; 2021 Feb; 43(2):115-121. PubMed ID: 33460028 [TBL] [Abstract][Full Text] [Related]
12. Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome. Kantaputra PN; Tanpaiboon P; Unachak K; Praphanphoj V Am J Med Genet A; 2004 Oct; 130A(2):181-90. PubMed ID: 15372530 [TBL] [Abstract][Full Text] [Related]
13. Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect. Meng L; Tu C; Lu G; Lin G; Tan Y Sci China Life Sci; 2019 Jan; 62(1):144-147. PubMed ID: 29961235 [No Abstract] [Full Text] [Related]
14. Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type II. Ozawa H; Takayama C; Nishida A; Nagai T; Nishimura G; Higurashi M Brain Dev; 2005 Apr; 27(3):237-40. PubMed ID: 15737708 [TBL] [Abstract][Full Text] [Related]
15. Osteodysplastic primordial dwarfism: a case with features of type II. Masuno M; Imaizumi K; Nishimura G; Kurosawa K; Makita Y; Shimazaki Y; Kuroki Y Clin Dysmorphol; 1995 Jan; 4(1):57-62. PubMed ID: 7735506 [TBL] [Abstract][Full Text] [Related]
16. Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I. Abdel-Salam GM; Abdel-Hamid MS; Issa M; Magdy A; El-Kotoury A; Amr K Am J Med Genet A; 2012 Jun; 158A(6):1455-61. PubMed ID: 22581640 [TBL] [Abstract][Full Text] [Related]
17. Further delineation of the clinical spectrum in RNU4ATAC related microcephalic osteodysplastic primordial dwarfism type I. Abdel-Salam GM; Abdel-Hamid MS; Hassan NA; Issa MY; Effat L; Ismail S; Aglan MS; Zaki MS Am J Med Genet A; 2013 Aug; 161A(8):1875-81. PubMed ID: 23794361 [TBL] [Abstract][Full Text] [Related]
18. Neurologic aspects of microcephalic osteodysplastic primordial dwarfism type II. Galasso C; Lo-Castro A; Lalli C; Cerminara C; Curatolo P Pediatr Neurol; 2008 Jun; 38(6):435-8. PubMed ID: 18486828 [TBL] [Abstract][Full Text] [Related]
19. Cutaneous features associated with microcephalic osteodysplastic primordial dwarfism type II. Webber N; O'Toole EA; Paige DG; Rosser E Pediatr Dermatol; 2008; 25(3):401-2. PubMed ID: 18577061 [TBL] [Abstract][Full Text] [Related]
20. A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II. Liu H; Tao N; Wang Y; Yang Y; He X; Zhang Y; Zhou Y; Liu X; Feng X; Sun M; Xu F; Su Y; Li L Mol Genet Genomic Med; 2021 Sep; 9(9):e1761. PubMed ID: 34331829 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]