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American Journal of Human Genetics|December 1, 1991
Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2)F Greenberg, V Guzzetta, R Montes de Oca-Luna, et al.Journal of Medical Genetics|October 4, 2002
"Molecular rulers" for calibrating phenotypic effects of telomere imbalanceC L Martin, D J Waggoner, A Wong, et al.Annals of Neurology|August 12, 1999
Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13P L Kramer, M Mineta, C Klein, et al.Human Mutation|October 26, 1999
Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndromeL A Schimmenti, H H Shim, J D Wirtschafter, et al.Journal of Medical Genetics|July 11, 2006
The cardiofaciocutaneous syndromeA Roberts, J Allanson, S K Jadico, et al.American Journal of Medical Genetics|November 1, 1986
New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndromeJ F Reynolds, G Neri, J P Herrmann, et al.American Journal of Medical Genetics. Supplement|January 1, 1987
The Montana Fetal Genetic Pathology Program and a review of prenatal death in humansJ M Opitz, J M FitzGerald, J F Reynolds, et al.Birth Defects Original Article Series|January 1, 1977
Grebe chondrodysplasia and similar forms of severe short-limbed dwarfismG Romeo, J Zonana, R S Lachman, et al.American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.American Journal of Medical Genetics|January 1, 1991
A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, et al.Pageof 40