Methotrexate and reproduction in men: Case report and recommendations von Morris, Laura F., Harrod, Mary J., Menter, M. Alan, Silverman, Alan K.

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Fryns syndrome: prenatal diagnosis and pathologic correlation von Sheffield, J S, Twickler, D M, Timmons, C, Land, K, Harrod, M J, Ramus, R M

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Risk of chromosomal abnormalities with emphasis on live-born offspring of young mothers von LITTLE, B. B, RAMIN, S. M, CAMBRIDGE, B. S, SCHNEIDER, N. R, COHEN, D. S, SNELL, L. M, HARROD, M. J, JOHNSTON, W. L

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Complementary duplication and deletion of 17 (pcen→p11.2): A family with a supernumerary chromosome comprised of an interstitially deleted segment von Friedman, J. M., Harrod, M. J. E., Howard-Peebles, P. N.

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Genetic Counseling for Usher's Syndrome Patients and Their Families von Harrod, M. J. E.

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Anatomic correlates of ultrasonographic prenatal diagnosis von Rutledge, Joe C., Weinberg, Arthur G., Friedman, Jan M., Harrod, Mary Jo, Santos-Ramos, Rigoberto

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Verification of the fetal valproate syndrome phenotype von Ardinger, Holly H., Atkin, Joan F., Blackston, R. Dwain, Elsas, Louis J., Clarren, Sterling K., Livingstone, Susan, Flannery, David B., Pellock, John M., Harrod, Mary Jo, Lammer, Edward J., Majewski, Frank, Schinzel, Albert, Toriello, Helga V., Hanson, James W., Optiz, John M., Reynolds, James F.

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Sternal malformation/vascular dysplasia association von Hersh, J. H., Waterfill, D., Rutledge, J., Harrod, M. J. E., O'sheal, S. F., Verdi, G., Martinez, S., Weisskopf, B., Opitz, John M., Reynolds, James F.

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Childhood allergy von Halpern, S R, Brasher, G W, Harrod, M J

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Del(20p) with manifestations of arteriohepatic dysplasia von Byrne, J. L. B., Harrod, M. J. E., Friedman, J. M., Howard-Peebles, P. N., Opitz, John M., Reynolds, James F.

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WARFARIN EMBRYOPATHY IN SIBLINGS von Harrod, M J E, Sherrod, P S

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Further delineation of Weaver syndrome von Ardinger, Holly H., Hanson, James W., Harrod, Mary Jo E., Cohen, M. Michael, Tibbles, John A.R., Welch, J. Philip, Young-Wee, Theresa, Sommer, Annemarie, Goldberg, Rosalie, Shprintzen, Robert J., Sidoti, Eugene J., Leichtman, Lawrence G., Hoyme, H. Eugene

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Congenital cataracts in mother, sister, and son of a patient with Hallermann-Streiff syndrome: Coincidence or clue? von Jo Harrod, Mary, Friedman, Jan M.

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Etiologic heterogeneity of fetal hydrocephalus diagnosed by ultrasound von Harrod, M.J.E., Friedman, J.M., Santos-Ramos, R., Rutledge, J., Weinberg, A.

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A "new" lethal multiple congenital anomaly syndrome: Joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnorm... von Rutledge, Joe C., Friedman, J. M., Harrod, M. J. E., Currarino, G., Wright, C. G., Pinckney, L., Chen, H.

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Genetic heterogeneity in spondyloepiphyseal dysplasia congenita von Harrod, Mary Jo E., Friedman, Jan M., Currarino, Guido, Pauli, Richard M., Langer Jr, Leonard O., Opitz, John M.

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Duplication 12q mosaicism in two unrelated patients with a similar syndrome von Harrod, M. J. E., Byrne, J. B., Dev, V. G., Francke, Uta, Optiz, John M.

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Ring 17 chromosome detected by amniocentesis von Weinberg, Arthur G., Bair, Janice L., Harrod, Mary Jo

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Genetic misconceptions von Friedman, J M, Harrod, M J

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Homozygous familial hypercholesterolemia: specificity of the biochemical defect in cultured cells and feasibility of prenatal detection von Goldstein, J L, Harrod, M J, Brown, M S

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