LL
Lawrence Leichtman
Medical Genetics / Clinical Genetics (M.D.)
Credentials: ·
Research
Multiple congenital anomalies associated with weekly low-dose methotrexate treatment of the mother
Case report · Arthritis & Rheumatism · 1997 · 112 citations
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
Nature Genetics · 1995 · 94 citations
Case report · American Journal of Medical Genetics · 1994 · First of 3 authors · 23 citations
2 papers
- AW
1 paper
- CB
1 paper
- EC
1 paper
- ES
1 paper
1 paper · 1 as a resident
- KA
1 paper
- LB
1 paper
