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Journal of Medical Genetics|February 1, 1985
Reduced penetrance in tuberous sclerosisM Baraitser, M A PattonJournal of Medical Genetics|April 1, 1986
A Noonan-like short stature syndrome with sparse hairM Baraitser, M A PattonJournal of Medical Genetics|September 1, 1987
The clinical spectrum of the Fraser syndrome: report of three new cases and reviewJ Gattuso, M A Patton, M BaraitserClinical Genetics|February 1, 1986
A family with congenital suprabulbar paresis (Worster-Drought syndrome)M A Patton, M Baraitser, E M BrettJournal of Medical Genetics|April 1, 1985
The clinical features of the Cohen syndrome: further case reportsC North, M A Patton, M Baraitser, et al.Journal of Medical Genetics|June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic featuresM A Patton, K D McDermot, B D Lake, et al.Journal of Medical Genetics|February 1, 1987
An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findingsM A Patton, M Baraitser, A H Heagerty, et al.Prenatal Diagnosis|March 1, 1986
Prenatal treatment of fetal hydrops associated with the hypertelorism-dysphagia syndrome (Opitz-G syndrome)M A Patton, M Baraitser, K Nickolaides, et al.American Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.Journal of Medical Genetics|May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?R M Winter, M A Patton, J Challener, et al.Pageof 23