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Pediatric Research|March 24, 1999
Reconstructing the history of human limb development: lessons from birth defectsM Bamshad, W S Watkins, M E Dixon, et al.
Genetic Epidemiology|January 1, 1986
Linkage analysis of Von Recklinghausen neurofibromatosis: chromosomes 4 and 19J N Dietz, T Robbins, L A Cannon, et al.
American Journal of Medical Genetics|November 15, 1993
Radiological features in Brachmann-de Lange syndromeS R Braddock, R S Lachman, C C Stoppenhagen, et al.
American Journal of Medical Genetics|October 23, 1997
Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individualsS B Bleyl, B R Mumford, M C Brown-Harrison, et al.
American Journal of Obstetrics and Gynecology|January 1, 1995
The impact of cocaine and marijuana use on low birth weight and preterm birth: a multicenter studyP H Shiono, M A Klebanoff, R P Nugent, et al.
American Journal of Medical Genetics|January 1, 1987
Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethalityC J Curry, J C Carey, J S Holland, et al.
American Journal of Human Genetics|December 1, 1994
A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9M Bamshad, W S Watkins, R K Zenger, et al.
American Journal of Human Genetics|July 1, 1995
Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patientsM C Lowery, C A Morris, A Ewart, et al.
Cell|July 13, 1990
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locusD Viskochil, A M Buchberg, G Xu, et al.
The Journal of Pediatrics|September 17, 1998
Costello syndrome: phenotype, natural history, differential diagnosis, and possible causeJ P Johnson, M Golabi, M E Norton, et al.
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