LawrenceGeneLeichtmanMD

PubMed

• 3 citations
  Prenatal detection of an inverted X chromosome in a male.
  Arthur R. Brothman, Anna Newlin, Susan E. Phillips, Gretchen Q. Kinzie, Lawrence G. Leichtman> ;Clinical Genetics. 2008 Apr 23
• 4 citations
  Ophthalmologic findings in the Dubowitz syndrome.
  William S Rodden, Earl R. Crouch, Lawrence G Leichtman, Herbert C Becker> ;Journal of Pediatric Ophthalmology and Strabismus. 1999 Jan 1
• 103 citations
  Multiple congenital anomalies associated with weekly low‐dose methotrexate treatment of the mother
  Lenore M. Buckley, Charles A. Bullaboy, Lawrence G. Leichtman, Mariella Marquez> ;Arthritis and Rheumatism. 1997 May 1
• 15 citations
  Hereditary Thyroglossal Duct Cysts
  John H. Greinwald, Leichtman Lg, Eric J. Simko> ;Archives of Otolaryngology--Head & Neck Surgery. 1996 Oct 1
• 15 citations
  Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: Case report and comparison with trisomy 9p
  Lawrence G. Leichtman, Joleen L. Zackowski, Patrick D. Storto, Anna Newlin> ;American Journal of Medical Genetics. 1996 Jun 14
• 86 citations
  Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.
  Nathaniel H. Robin, George J. Feldman, A L Aronson, H F Mitchell, Rosanna Weksberg, Claire O. Leonard, Barbara K. Burton, Kevin D. Josephson, Renata Laxova, Kyrieckos ...> ;Nature Genetics. 1995 Dec 1
• 20 citations
  Anophthalmia, cleft lip/palate, facial anomalies, and CNS anomalies and hypothalamic disorder in a newborn: a midline developmental field defect
  Lawrence G. Leichtman, Brian Wood, Reuben D. Rohn> ;American Journal of Medical Genetics. 1994 Mar 1
• 13 citations
  Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25)
  Lawrence G. Leichtman, Daniel Strum, Arthur R. Brothman> ;American Journal of Medical Genetics. 1993 Mar 15
• 20 citations
  Apparent Opitz BBBG syndrome with a partial duplication of 5p.
  Lawrence G. Leichtman, A Werner, W T Bass, D Smith, Arthur R. Brothman> ;American Journal of Medical Genetics. 1991 Aug 1
• 63 citations
  Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin.
  Nancy J. Carpenter, Lawrence G. Leichtman, Burhan Say> ;American Journal of Diseases of Children. 1982 May 1
• 1 citations
  Primary pulmonary hypoplasia and arthrogryposis multiplex congenita
  Lawrence G. Leichtman, Burhan Say, Nancy Barber> ;The Journal of Pediatrics. 1980 May 1
• 12 citations
  Ankylosis, facial anomalies, and pulmonary hypoplasia syndrome.
  Burhan Say, Nancy Barber, Lawrence G. Leichtman> ;American Journal of Diseases of Children. 1979 Nov 1
• Trisomy 1q42qter "syndrome": additional case report.
  Storto, P., Zackowski, J., Leichtman, L., Montgomery, T., Newlin, A.> ;Am J Med Genet. 2001 Mar 15
• Are cardio-facio-cutaneous syndrome and Noonan syndrome distinct? A case of CFC offspring of a mother with Noonan syndrome.
  Leichtman, L. G.> ;Clin Dysmorphol. 1996 Jan
• An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?
  Carpenter, N. J., Leichtman, L. G., Stamper, S., Say, B.> ;J Med Genet. 1981 Jun
• The Gordon syndrome.
  Say, B., Barber, D. H., Thompson, R. C., Leichtman, L. G.> ;J Med Genet. 1980 Oct
• Patients in a clinic for children with multiple handicaps: a retrospective diagnostic evaluation.
  Leichtman, L. G., Say, B., Coldwell, J. G.> ;South Med J. 1980 Sep
• Proficiency testing for biochemical genetics laboratories: the first 10 rounds of testing.
  Hommes, F. A., Brewster, M. A., Burton, B. K., Buist, N. R., Elsas, L. J., Goldsmith, B. M., Hammond, J., Kruckeberg, W. C., Leichtman, L. G., Lin, K. T.> ;Am J Hum Genet. 1990 May
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