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American Journal of Medical Genetics|June 9, 1999
Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluationL G Biesecker, R Happle, J B Mulliken, et al.
The Journal of Hand Surgery|July 1, 1989
Aeromonas hydrophila infection complicating digital replantation and revascularizationR M Lowen, C M Rodgers, L L Ketch, et al.
The Journal of Pediatrics|September 1, 1996
Hepatic vascular anomalies in infancy: a twenty-seven-year experienceL M Boon, P E Burrows, H J Paltiel, et al.
The Journal of Pediatrics|April 17, 1998
Spastic diplegia as a complication of interferon Alfa-2a treatment of hemangiomas of infancyC F Barlow, C J Priebe, J B Mulliken, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 20, 2001
Craniofacial, temporal bone, and audiologic abnormalities in the spectrum of hemifacial microsomiaR Rahbar, C D Robson, J B Mulliken, et al.
AJNR. American Journal of Neuroradiology|February 14, 2009
Infantile hemangiomas involving the neuraxis: clinical and imaging findingsV Viswanathan, E R Smith, J B Mulliken, et al.
Radiology|June 4, 1998
Cerebral vasculopathy and neurologic sequelae in infants with cervicofacial hemangioma: report of eight patientsP E Burrows, R L Robertson, J B Mulliken, et al.
AJNR. American Journal of Neuroradiology|February 12, 2011
Complex spinal-paraspinal fast-flow lesions in CLOVES syndrome: analysis of clinical and imaging findings in 6 patientsA I Alomari, G Chaudry, G Rodesch, et al.
American Journal of Human Genetics|June 12, 1999
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22L M Boon, P Brouillard, A Irrthum, et al.
AJNR. American Journal of Neuroradiology|October 20, 2000
Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnosesC D Robson, J B Mulliken, R L Robertson, et al.
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