Cunningham ML - Search Results

1

Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.

Paznekas WA, Cunningham ML, Howard TD, Korf BR, Lipson MH, Grix AW, Feingold M, Goldberg R, Borochowitz Z, Aleck K, Mulliken J, Yin M, Jabs EW. Paznekas WA, et al. Among authors: cunningham ml. Am J Hum Genet. 1998 Jun;62(6):1370-80. doi: 10.1086/301855. Am J Hum Genet. 1998. PMID: 9585583 Free PMC article.

2

Another TWIST on Baller-Gerold syndrome.

Seto ML, Lee SJ, Sze RW, Cunningham ML. Seto ML, et al. Among authors: cunningham ml. Am J Med Genet. 2001 Dec 15;104(4):323-30. doi: 10.1002/ajmg.10065. Am J Med Genet. 2001. PMID: 11754069 Review.

3

Century of Jackson-Weiss syndrome: further definition of clinical and radiographic findings in "lost" descendants of the original kindred.

Heike C, Seto M, Hing A, Palidin A, Hu FZ, Preston RA, Ehrlich GD, Cunningham M. Heike C, et al. Am J Med Genet. 2001 May 15;100(4):315-24. doi: 10.1002/ajmg.1266. Am J Med Genet. 2001. PMID: 11343323

4

Syndromic craniosynostosis: from history to hydrogen bonds.

Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV. Cunningham ML, et al. Orthod Craniofac Res. 2007 May;10(2):67-81. doi: 10.1111/j.1601-6343.2007.00389.x. Orthod Craniofac Res. 2007. PMID: 17552943 Review.

5

Pulmonary agenesis: a predictor of ipsilateral malformations.

Cunningham ML, Mann N. Cunningham ML, et al. Am J Med Genet. 1997 Jun 27;70(4):391-8. doi: 10.1002/(sici)1096-8628(19970627)70:4<391::aid-ajmg11>3.0.co;2-c. Am J Med Genet. 1997. PMID: 9182780 Review.

6

Pathogenesis of ectrodactyly in the Dactylaplasia mouse: aberrant cell death of the apical ectodermal ridge.

Seto ML, Nunes ME, MacArthur CA, Cunningham ML. Seto ML, et al. Among authors: cunningham ml. Teratology. 1997 Oct;56(4):262-70. doi: 10.1002/(SICI)1096-9926(199710)56:4<262::AID-TERA5>3.0.CO;2-0. Teratology. 1997. PMID: 9408977

7

Hemifacial myohyperplasia: description of a new syndrome.

Lee S, Sze R, Murakami C, Gruss J, Cunningham M. Lee S, et al. Am J Med Genet. 2001 Nov 1;103(4):326-33. Am J Med Genet. 2001. PMID: 11746014

8

Medical treatment of craniosynostosis: recombinant Noggin inhibits coronal suture closure in the rat craniosynostosis model.

Shen K, Krakora SM, Cunningham M, Singh M, Wang X, Hu FZ, Post JC, Ehrlich GD. Shen K, et al. Orthod Craniofac Res. 2009 Aug;12(3):254-62. doi: 10.1111/j.1601-6343.2009.01460.x. Orthod Craniofac Res. 2009. PMID: 19627528 Free PMC article.

9

Transmission of the dysgnathia complex from mother to daughter.

Erlich MS, Cunningham ML, Hudgins L. Erlich MS, et al. Among authors: cunningham ml. Am J Med Genet. 2000 Nov 27;95(3):269-74. Am J Med Genet. 2000. PMID: 11102934

10

Revisiting a Rare Anomaly Described 25 Years Ago in the AJNR: A Journey from Pediatric Hemifacial Microsomia and Middle Cranial Fossa Aplasia to CSF-Lymphatic Fistula and Spontaneous Intracranial Hypotension as an Adult.

Callen AL, Khanwalkar AR, Cunningham ML, Pisani Petrucci SL, Bhaumik D, Wilhour D, Trivedi P, Lennarson P, Zander DA. Callen AL, et al. Among authors: cunningham ml. AJNR Am J Neuroradiol. 2025 Mar 27:ajnr.A8760. doi: 10.3174/ajnr.A8760. Online ahead of print. AJNR Am J Neuroradiol. 2025. PMID: 40147836

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

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

321 results

Search Page

Filters