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Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.
American Journal of Perinatology|November 1, 1993
Association of clinical intra-amniotic infection and meconiumT S Wen, N L Eriksen, J D Blanco, et al.
American Journal of Surgery|December 1, 1982
Carotid artery injuriesM F Brown, J M Graham, D V Feliciano, et al.
American Journal of Human Genetics|July 11, 1990
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markersJ H Knoll, R D Nicholls, R E Magenis, et al.
The Journal of Laryngology and Otology. Supplement|January 1, 1989
UCH/RNID single channel extracochlear implant: results in thirty profoundly deafened adultsH R Cooper, L Carpenter, W Aleksy, et al.
The Journal of Trauma|September 1, 1987
Delayed posterior internal fixation of unstable pelvic fracturesB D Browner, J D Cole, J M Graham, et al.
Prenatal Diagnosis|April 1, 1994
Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16A Garber, D Carlson, R Schreck, et al.
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.
Prenatal Diagnosis|October 1, 1993
Preaxial ray reduction defects as part of valproic acid embryofetopathyR Sharony, A Garber, D Viskochil, et al.
The Journal of Clinical Investigation|October 1, 1989
Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotypeB J Starman, D Eyre, H Charbonneau, et al.
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