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American Journal of Medical Genetics|May 1, 1989
Wisconsin consanguinity studies. II: Familial adenocarcinomatosisR R Lebel, W B GallagherAmerican Journal of Medical Genetics|May 1, 1989
Weaver syndrome: the changing phenotype in an adultF Greenberg, W Wasiewski, E R McCabeAmerican Journal of Medical Genetics|May 1, 1989
Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndromeU Tantravahi, R D Nicholls, H Stroh, et al.American Journal of Medical Genetics|August 1, 1989
Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new AFD syndrome?A Richieri-Costa, M L Guion-AlmeidaAmerican Journal of Medical Genetics|August 1, 1989
Microdeletion in the X-chromosome and prenatal diagnosis in a family with Norrie diseaseD P Zhu, S E Antonarakis, B J Schmeckpeper, et al.American Journal of Medical Genetics|August 1, 1989
Growth and development in thanatophoric dysplasiaI M MacDonald, A G Hunter, P M MacLeod, et al.American Journal of Medical Genetics|August 1, 1989
Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden deathV E Shih, S M Axel, J C Tewksbury, et al.American Journal of Medical Genetics|November 1, 1989
Multiple malformations and exposure to therapeutic ultrasound during organogenesisD R McLeod, S B FowlowAmerican Journal of Medical Genetics|November 1, 1989
Expanded phenotype and ethnicity in Setleis syndromeR D Clark, M Golabi, Y Lacassie, et al.American Journal of Medical Genetics|November 1, 1989
Re-evaluation of new X-linked syndrome for evidence of CHARGE syndrome or associationM A Abruzzo, R P EricksonPageof 854