Similar articles for PMID: 26818173

Year	Number of Results
1971	1
1973	1
1974	1
1976	1
1977	1
1978	1
1979	2
1983	1
1984	2
1985	1
1986	1
1987	2
1988	2
1989	1
1990	2
1992	5
1993	4
1994	5
1995	4
1996	3
1997	2
1998	4
2000	1
2001	1
2002	4
2003	2
2004	3
2006	4
2007	3
2008	4
2009	2
2010	3
2011	7
2012	4
2013	4
2014	3
2015	3
2016	3
2017	1
2018	1
2019	4
2020	2
2021	2
2024	0

1

Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder.

Abu-Amero KK, Kondkar AA, Hellani AM, Bosley TM, Khan AO. Abu-Amero KK, et al. Neurosciences (Riyadh). 2016 Jan;21(1):72-4. doi: 10.17712/nsj.2016.1.20150098. Neurosciences (Riyadh). 2016. PMID: 26818173 Free PMC article. No abstract available.

2

An autosomal dominantly inherited syndrome of facial asymmetry, esotropia, amblyopia, and submucous cleft palate (Bencze syndrome).

Kurnit D, Hall JG, Shurtleff DB, Cohen MM Jr. Kurnit D, et al. Clin Genet. 1979 Nov;16(5):301-4. doi: 10.1111/j.1399-0004.1979.tb01006.x. Clin Genet. 1979. PMID: 519901

3

Microdeletion of chromosome 7P syndrome ocular manifestations.

Cartwright MJ, Hassan TS, Frueh BR. Cartwright MJ, et al. Ophthalmic Plast Reconstr Surg. 1995 Jun;11(2):139-41. doi: 10.1097/00002341-199506000-00012. Ophthalmic Plast Reconstr Surg. 1995. PMID: 7654619

4

Monozygotic twins with 22q11 deletion and discordant phenotypes.

Fryer A. Fryer A. J Med Genet. 1996 Feb;33(2):173. doi: 10.1136/jmg.33.2.173. J Med Genet. 1996. PMID: 8929959 Free PMC article. No abstract available.

5

Ocular and systemic findings in the Aarskog (facial-digital-genital) syndrome.

Brodsky MC, Keppen LD, Rice CD, Ranells JD. Brodsky MC, et al. Am J Ophthalmol. 1990 Apr 15;109(4):450-6. doi: 10.1016/s0002-9394(14)74612-4. Am J Ophthalmol. 1990. PMID: 2330948

6

Absence of a lateral rectus muscle associated with duplication of the chromosome segment 7q32----q34.

Keith CG, Webb GC, Rogers JG. Keith CG, et al. J Med Genet. 1988 Feb;25(2):122-5. doi: 10.1136/jmg.25.2.122. J Med Genet. 1988. PMID: 3346885 Free PMC article.

7

Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome.

Khan AO, Shinwari J, Al Sharif L, Khalil D, Al-Gehedan S, Tassan NA. Khan AO, et al. Mol Vis. 2011;17:1997-2002. Epub 2011 Jul 20. Mol Vis. 2011. PMID: 21850174 Free PMC article.

8

X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome.

Møller RS, Jensen LR, Maas SM, Filmus J, Capurro M, Hansen C, Marcelis CL, Ravn K, Andrieux J, Mathieu M, Kirchhoff M, Rødningen OK, de Leeuw N, Yntema HG, Froyen G, Vandewalle J, Ballon K, Klopocki E, Joss S, Tolmie J, Knegt AC, Lund AM, Hjalgrim H, Kuss AW, Tommerup N, Ullmann R, de Brouwer AP, Strømme P, Kjaergaard S, Tümer Z, Kleefstra T. Møller RS, et al. Hum Genet. 2014 May;133(5):625-38. doi: 10.1007/s00439-013-1403-3. Epub 2013 Dec 11. Hum Genet. 2014. PMID: 24326587

9

Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.

Garganta CL, Bodurtha JN. Garganta CL, et al. Am J Med Genet. 1992 Sep 15;44(2):129-35. doi: 10.1002/ajmg.1320440202. Am J Med Genet. 1992. PMID: 1456279 Review.

10

Familial Recurrence of 3MC Syndrome in Consanguineous Families: A Clinical and Molecular Diagnostic Approach With Review of the Literature.

Gardner OK, Haynes K, Schweitzer D, Johns A, Magee WP, Urata MM, Sanchez-Lara PA. Gardner OK, et al. Cleft Palate Craniofac J. 2017 Nov;54(6):739-748. doi: 10.1597/15-151. Epub 2016 Jun 29. Cleft Palate Craniofac J. 2017. PMID: 27356087 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

101 results

Results by year