Lawrence G. Leichtman

Multiple congenital anomalies associated with weekly low‐dose methotrexate treatment of the mother

Lenore M. Buckley, Charles A. Bullaboy, Lawrence G. Leichtman et al. · Arthritis & Rheumatism · 1997 · 149 citations · Full text

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

Nathaniel H. Robin, George Feldman, Adam Aronson et al. · Nature Genetics · 1995 · 122 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Further delineation of Weaver syndrome

Holly H Ardinger, James W. Hanson, Mary Jo Harrod et al. · The Journal of Pediatrics · 1986 · 51 citations

Weaver Syndrome, Genetics, Mendelian Disorder +1

An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?

Nancy J. Carpenter, Lawrence G. Leichtman, S Stamper et al. · Journal of Medical Genetics · 1981 · 28 citations · Full text

Cytogenetics, Dermatoglyphic, Pathology +17

Are cardio-facio-cutaneous syndrome and Noonan syndrome distinct? A case of CFC offspring of a mother with Noonan syndrome

Lawrence G. Leichtman · Clinical Dysmorphology · 1996 · 28 citations

Cfc Offspring, Cardio-facio-cutaneous Syndrome, Are Cardio-facio-cutaneous Syndrome +6