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K M Gustashaw

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American Journal of Human Genetics|May 1, 1992
The presence of interstitial telomeric sequences in constitutional chromosome abnormalitiesV M Park, K M Gustashaw, T M Wathen
Prenatal Diagnosis|October 1, 1989
Prenatal diagnosis of Turner syndrome using cells cultured from cystic hygromas in two pregnancies with normal maternal serum alpha-fetoproteinW L Golden, B F Schneider, K M Gustashaw, et al.
Methods in Cell Biology|January 1, 1982
Prenatal cytogenetic diagnosisM M Sandstrom, M T Beauchesne, K M Gustashaw, et al.
American Journal of Medical Genetics|November 1, 1991
Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomesV M Park, K M Gustashaw, R M Bilenker, et al.
American Journal of Medical Genetics|October 15, 1994
Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivationK M Gustashaw, V Zurcher, L H Dickerman, et al.
Human Genetics|August 1, 1997
Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation patternD J Wolff, K M Gustashaw, V Zurcher, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Human Genetics|May 1, 1992
The presence of interstitial telomeric sequences in constitutional chromosome abnormalitiesV M Park, K M Gustashaw, T M Wathen
Prenatal Diagnosis|October 1, 1989
Prenatal diagnosis of Turner syndrome using cells cultured from cystic hygromas in two pregnancies with normal maternal serum alpha-fetoproteinW L Golden, B F Schneider, K M Gustashaw, et al.
Methods in Cell Biology|January 1, 1982
Prenatal cytogenetic diagnosisM M Sandstrom, M T Beauchesne, K M Gustashaw, et al.
American Journal of Medical Genetics|November 1, 1991
Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomesV M Park, K M Gustashaw, R M Bilenker, et al.
American Journal of Medical Genetics|October 15, 1994
Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivationK M Gustashaw, V Zurcher, L H Dickerman, et al.
Human Genetics|August 1, 1997
Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation patternD J Wolff, K M Gustashaw, V Zurcher, et al.
Pageof 1