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Neurology|July 17, 1999
Familial trigeminal neuralgia and contralateral hemifacial spasmJ M Duff, R J Spinner, N M Lindor, et al.
American Journal of Medical Genetics|October 6, 1999
CALL gene is haploinsufficient in a 3p- syndrome patientD Angeloni, N M Lindor, S Pack, et al.
Gynecologic Oncology|October 8, 2003
Pelvic primitive neuroectodermal tumor associated with a cluster of small round cell tumors: case report and review of current literatureBobbie S Gostout, Noralane M Lindor, Connie S DiMarco, et al.
American Journal of Medical Genetics|December 18, 1998
Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: another ophthalmologic complicationD Babovic-Vuksanovic, S M Jalal, J A Garrity, et al.
American Journal of Medical Genetics|March 15, 1994
Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenicsN M Lindor, J L Sobell, L L Heston, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
A preliminary investigation of genetic counselors' information needs when receiving a variant of uncertain significance result: a mixed methods studyCourtney L Scherr, Noralane M Lindor, Teri L Malo, et al.
Clinical Genetics|June 4, 1998
Maternal cell contamination of buccal smear samples in nursing neonatesD Babovic-Vuksanovic, V V Michels, M E Law, et al.
The British Journal of Dermatology|June 20, 2002
Progressive extensive osteoma cutis associated with dysmorphic features: a new syndrome? Case report and review of the literatureM D P Davis, M R Pittelkow, N M Lindor, et al.
American Journal of Medical Genetics|April 27, 2002
Confirmation of existence of a new syndrome: LAPS syndromeNoralane M Lindor, Jan L Kasperbauer, Alan D Hoffman, et al.
European Journal of Human Genetics : EJHG|January 23, 2014
Fragile X syndrome due to a missense mutationLeila K Myrick, Mika Nakamoto-Kinoshita, Noralane M Lindor, et al.
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