Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocation von Author, An

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Toluene embryopathy von Hersh, Joseph H., Podruch, Philip E., Rogers, George, Weisskopf, Bernard

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A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation von Yen, F S, Podruch, P E, Weisskopf, B

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Computed tomography of the head in the evaluation of microcephaly von JAWORSKI, M, HERSH, J. H, DONAT, J, SHEARER, L. T, WEISSKOPF, B

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Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardation von Podruch, P E, Yen, F S, Dinno, N D, Weisskopf, B

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A Case of Familial XY Gonadal Dysgenesis von Hersh, Joseph H., Kable, Warren Tim, Yen, Frank Fusen, Yussman, Marvin A., Weisskopf, Bernard

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An unusual case of short limbed dwarfism and thoracic dystrophy with normal spine, hands and feet von Dinno, N D, Shearer, L T, Weisskopf, B

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Syndrome of Growth Resistance, Obesity, and Intellectual Impairment with Precocious Puberty von Macmillan, Duncan R., Bin Kim, Chong, Weisskopf, Bernard

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Forearm fullness in Coffin-Lowry syndrome: A misleading yet possible early diagnostic clue von Hersh, Joseph H., Weisskopf, Bernard, DeCoster, Crystal, Opitz, John M.

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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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Learning disorders in children: behavioral and emotional aspects of child and family von Weisskopf, B

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Methylphenidate-induced Delusional Disorder in A Child With Attention Deficit Disorder With Hyperactivity von BLOOM, ALLAN S., RUSSELL, LAURA J., WEISSKOPF, BERNARD, BLACKERBY, JEFFRIES L.

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Ivemark's "asplenia" syndrome: a single gene disorder von McChane, R H, Hersh, J H, Russell, L J, Weisskopf, B

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Three different, non-mosaic sex chromosome abnormalities (direct cytotrophoblasts, mesenchymal core cultures, and abortus skin fibroblasts): implications for elucidating chorionic... von Shulman, L P, Tharapel, A T, Simpson, J L, Meyers, C M, Tucker, B, Weisskopf, B, Elias, S

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Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15p+;9q−) in three generations von Podruch, Philip E., Weisskopf, Bernard

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Clinical correlations in partial hypoxanthine guanine phosphoribosyltransferase deficiency von Hersh, Joseph H., Page, Theodore, Hand, Mary E., Edwin Seegmiller, J., Nyhan, William L., Weisskopf, Bernard

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Three different, non-mosaic sex chromosome abnormalities (direct cytotrophoblasts, mesenchymal core cultures, and abortus skin fibroblasts): implications for elucidating chorionic... von SHULMAN, L. P, THARAPEL, A. T, LEIGH SIMPSON, J, MEYERS, C. M, TUCKER, B, WEISSKOPF, B, ELIAS, S

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Townes Syndrome: A Distinct Multiple Malformation Syndrome Resembling VACTERL Association von Hersh, Joseph H., Jaworski, Margie, Solinger, Robert E., Weisskopf, Bernard, Donat, Jane

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Mild intellectual deficits in a child with 49,XXXXY von Hersh, Joseph H., Bloom, Allan S., Yen, Frank, Topinka, Carolyn, Weisskopf, Bernard

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Psychological Aspects of Cerebral Gigantism von Patterson, B., Bloom, A., Reese, A., Weisskopf, B.

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