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American Journal of Medical Genetics|July 1, 1994
Increased risk for type I (insulin-dependent) diabetes in relatives of patients with alopecia areata (AA)S J Wang, T Shohat, C Vadheim, et al.American Journal of Medical Genetics|July 1, 1994
Split hand/split foot, syndactyly, urinary tract obstruction, radial, diaphragmatic, and neural tube defects: Czeizel-Losonci syndrome?M Genuardi, E Silvestri, C TozziAmerican Journal of Medical Genetics|July 1, 1994
New syndrome: autosomal dominant microcephaly and radio-ulnar synostosisL Giuffrè, G Corsello, M Giuffrè, et al.American Journal of Medical Genetics|June 15, 1994
Family patterns of developmental dyslexia: clinical findingsP H Wolff, I MelngailisAmerican Journal of Medical Genetics|January 1, 1977
Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22qK M Taylor, U Francke, M G Brown, et al.American Journal of Medical Genetics|January 1, 1977
Isolated acid neuraminidase deficiency: a distinct lysosomal storage diseaseT E Kelly, G GraetzAmerican Journal of Medical Genetics|September 15, 1993
Is there a relationship between inborn errors of metabolism and extensive mongolian spots?H M Mendez, L I Pinto, G A Paskulin, et al.American Journal of Medical Genetics|September 15, 1993
Evaluation of families wherein a single male manifests a phenotype of X-linked lymphoproliferative disease (XLP)H L Grierson, J Skare, J Church, et al.American Journal of Medical Genetics|September 15, 1993
Metacarpophalangeal pattern profile analysis in Williams syndromeM A Burns, D R McLeod, L R Linton, et al.American Journal of Medical Genetics|September 15, 1993
Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletionR T Zori, J R Lupski, Z Heju, et al.Pageof 854