PubMed for id: 868099

Year	Number of Results
1984	1
1991	1
1995	1
1997	2
2001	1
2004	1
2005	1
2011	2
2012	1
2016	1
2018	1
2021	1
2024	0

1

Genotype-phenotype correlation of a 5q22.3 deletion associated with craniofacial and limb defects.

Lee S, Chae H, Park IY, Kim M, Kim Y, Shin JC, Lee J, Son J. Lee S, et al. Gene. 2012 Feb 15;494(1):105-8. doi: 10.1016/j.gene.2011.11.063. Epub 2011 Dec 8. Gene. 2012. PMID: 22178765

2

Terminal 6q25.3 deletion and abnormal behaviour.

Lukusa T, Willekens D, Lukusa N, De Cock F, Fryns JP. Lukusa T, et al. Genet Couns. 2001;12(3):213-21. Genet Couns. 2001. PMID: 11693783

3

Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family.

Mégarbané A, Tomey K, Wakim G. Mégarbané A, et al. Am J Med Genet. 1997 Nov 28;73(1):67-71. doi: 10.1002/(sici)1096-8628(19971128)73:1<67::aid-ajmg13>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9375925

4

Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report.

Hamel BC, Draaisma JM, Pinckers AJ, Boetes C, Hoppe RL, Ropers HH, Brunner HG. Hamel BC, et al. Am J Med Genet. 1995 Apr 10;56(3):312-6. doi: 10.1002/ajmg.1320560320. Am J Med Genet. 1995. PMID: 7778598 Free article. Review.

5

Congenital ocular fibrosis with musculoskeletal abnormality: a new association.

Kishore K, Kumar H. Kishore K, et al. J Pediatr Ophthalmol Strabismus. 1991 Sep-Oct;28(5):283-6. doi: 10.3928/0191-3913-19910901-12. J Pediatr Ophthalmol Strabismus. 1991. PMID: 1955966

6

Frank-ter Haar syndrome--additional findings?

Köse TE, İşler C, Şenel ŞN, Şitilci T, Özcan İ, Aksakallı N. Köse TE, et al. Dentomaxillofac Radiol. 2016;45(2):20150119. doi: 10.1259/dmfr.20150119. Dentomaxillofac Radiol. 2016. PMID: 26582053 Free PMC article.

7

Frank-Ter Haar Syndrome.

Saeed M, Shair QA, Saleem SM. Saeed M, et al. J Coll Physicians Surg Pak. 2011 Apr;21(4):252-3. J Coll Physicians Surg Pak. 2011. PMID: 21453629

8

Further delineation of Frank-ter Haar syndrome.

Maas SM, Kayserili H, Lam J, Apak MY, Hennekam RC. Maas SM, et al. Am J Med Genet A. 2004 Dec 1;131(2):127-33. doi: 10.1002/ajmg.a.30244. Am J Med Genet A. 2004. PMID: 15523657 Review.

9

A new multiple malformation syndrome of Müllerian dysgenesis and conductive hearing loss with facial hypoplasia, bilateral forearm deformity, brachydactyly, spinal stenosis and scoliosis.

Kumar D, Masel JP. Kumar D, et al. Clin Genet. 1997 Jul;52(1):30-6. doi: 10.1111/j.1399-0004.1997.tb02511.x. Clin Genet. 1997. PMID: 9272710

10

Poorly differentiated chordoma showing loss of SMARCB1/INI1: Clinicopathological and radiological spectrum of nine cases, including uncommon features of a relatively under-recognized entity.

Rekhi B, Michal M, Ergen FB, Roy P, Puls F, Haugland HK, Soylemezoglu F, Kosemehmetoglu K. Rekhi B, et al. Ann Diagn Pathol. 2021 Dec;55:151809. doi: 10.1016/j.anndiagpath.2021.151809. Epub 2021 Aug 27. Ann Diagn Pathol. 2021. PMID: 34482218

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 Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

13 results

Results by year

Filters

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

PubMed for id: 868099

13 results

Results by year