Human ETS2 Gene on Chromosome 21 is not Rearranged in Alzheimer disease von Sacchi, N., Nalbantoglu, J., Sergovich, F. R., Papas, T. S.

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Choroideremia associated with an X-autosomal translocation von SIU, V. M, GONDER, J. R, JUNG, J. H, SERGOVICH, F. R, FLINTOFF, W. F

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Prenatal diagnosis of 45,X/46,XY mosaicism in a fetus with asymmetric gonadal dysgenesis von Kirkilionis, A. J., Rodney, P., Sergovich, F. R., Armstrong, R.

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18q-mosaicism associated with Rett syndrome phenotype von Gordon, Kevin, Siu, Victoria Mok, Sergovich, Fred, Jung, Jack

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Gene expression and metastasis of somatic cell hybrids between murine fibroblast cell lines of different malignant potential von TUCK, A. B, WILSON, S. M, SERGOVICH, F. R, CHAMBERS, A. F

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Down syndrome with apparently normal chromosomes: An update von Kirkilionis, Angelika J., Sergovich, Frederick R.

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The triplo-X female: an appraisal based on a study of 12 cases and a review of the literature von Barr, M L, Sergovich, F R, Carr, D H, Saver, E L

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The 49,XXXXX chromosome constitution:Similarities to the 49,XXXXY condition von Sergovich, F., Uilenberg, Catharina, Pozsonyi, J.

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The Clinical Syndrome of Triploidy von WERTELECKI, WLADIMIR, GRAHAM, JOHN M., SERGOVICH, FRED R.

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Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata von Wertelecki, W., Breg, W. R., Graham Jr, J. M., Iinuma, K., Puck, S. M., Sergovich, F. R., Opitz, John M., Reynolds, James F.

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Infants undergoing antenatal genetic diagnosis: A preliminary report von Allen, H.H., Sergovich, F., Stuart, E.M., Pozsonyi, J., Murray, B.

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The growth and development of four XYY infants von Valentine, G H, McClelland, M A, Sergovich, F R

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The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene von Trifiro, Mark, Gottlieb, Bruce, Pinsky, Leonard, Kaufman, Morris, Prior, Lynn, Belsham, Denise D., Wrogemann, Klaus, Brown, Carolyn J., Willard, Huntington F., Trapman, Jan, Brinkmann, Albert O., Chang, Chawnshang, Liao, Shutsung, Sergovich, Fred, Jung, Jack

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A 13-15/21 translocation chromosome in carrier father and mongol son von SERGOVICH, F R, SOLTAN, H C, CARR, D H

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Annex 6: Chromosome mosaicism in CVS and amniocentesis samples von Teshima, I. E., Kalousek, D. K., Vekemans, M. J. J., Markovic, V., Cox, D. M., Dallaire, L., Gagne, R., Lin, J. C. C., Ray, M., Sergovich, F. R., Uchida, I. A., Wang, H., Tomkins, D. J.

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Genetics. CHROMOSOME ABERRATIONS IN 2159 CONSECUTIVE NEWBORN BABIES von SERGOVICH, F, VALENTINE, G H, CHEN, A T. L, KINCH, R A. H, SMOUT, M S

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Human ETS2 gene on chromosome 21 is not rearranged in Alzheimer disease von Sacchi, N, Nalbantoglu, J, Sergovich, F R, Papas, T S

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The D trisomy syndrome: a case report with a description of ocular pathology von SERGOVICH, F, MADRONICH, J S, BARR, M L, CARR, D H, LANGDON, W A

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Mongolism (Down's syndrome) with atypical clinical and cytogenetic features von Sergovich, Frederick R., Valentine, G. Howard, Carr, David H., Soltan, Hubert C.

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Prenatal diagnosisis of 45,X/46,XY mosaicism in a fetus with asymmetric gonadal dysgenesis von KIRKILIONIS, A. J, RODNEY, P, SERGOVICH, F. R, ARMSTRONG, R

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