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Seminars in Hematology|November 4, 1998
The DiGeorge anomaly (CATCH 22, DiGeorge/velocardiofacial syndrome)R HongAmerican Journal of Diseases of Children (1960)|September 1, 1990
Update on the immunodeficiency diseasesR HongTeratology|August 1, 1975
The role of beta-adrenergic activity in the production of cardiac and aortic arch anomalies in chick embryosR J Hodach, A E Hodach, J F Fallon, et al.Birth Defects Original Article Series|January 1, 1987
Management of the fetus with urinary tract dilatationR Laxova, L E Biesecker, R O Friday, et al.Birth Defects Original Article Series|January 1, 1977
The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemiaC H Gonzalez, M V Durkin-Stamm, N F Geimer, et al.American Journal of Medical Genetics|July 1, 1989
Spinocerebellar ataxia, hypogonadotropic hypogonadism, and choroidal dystrophy (Boucher-Neuhäuser syndrome)E R Limber, G H Bresnick, R M Lebovitz, et al.The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.Clinical Neuropathology|January 1, 1990
Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA)S M Chou, E F Gilbert, R W Chun, et al.American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatmentF Lalatta, D Clerici Bagozzi, M G Salmoiraghi, et al.European Journal of Human Genetics : EJHG|January 17, 2003
PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndromeM I Kavamura, M G Pomponi, M Zollino, et al.Pageof 57