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American Journal of Medical Genetics|December 1, 1987
Deletions of proximal 15q without Prader-Willi syndromeF Greenberg, D H LedbetterAmerican Journal of Medical Genetics|April 1, 1988
Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q)G E Herman, F Greenberg, D H LedbetterHuman Genetics|April 1, 1991
Determination of the origin of nondisjunction in a 49,XXXXY male using hypervariable dinucleotide repeat sequencesT H Huang, F Greenberg, D H LedbetterClinical Genetics|November 1, 1983
Cystic hygroma and hydrops fetalis in a fetus with trisomy 13F Greenberg, R J Carpenter, D H LedbetterAmerican Journal of Medical Genetics|October 1, 1991
Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1]L C Surh, D H Ledbetter, F GreenbergAmerican Journal of Medical Genetics|December 1, 1987
Neonatal diagnosis of Prader-Willi syndrome and its implicationsF Greenberg, F F Elder, D H LedbetterAmerican Journal of Medical Genetics|March 1, 1993
Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardationL G Shaffer, J T Hecht, D H Ledbetter, et al.Human Genetics|August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13A L Pettigrew, F Greenberg, C T Caskey, et al.American Journal of Human Genetics|November 1, 1988
Cytogenetic findings in a prospective series of patients with DiGeorge anomalyF Greenberg, F F Elder, P Haffner, et al.American Journal of Medical Genetics|August 1, 1991
Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2)J R Lupski, C Langston, R Friedman, et al.Pageof 33