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E C Jenkins

Showing results (51-60 of 146) with videos related to

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American Journal of Medical Genetics|April 1, 1992
Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairmentW T Brown, E C Jenkins, P Goonewardena, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|November 1, 1989
Parent-child dyadic gaze patterns in fragile X males and in non-fragile X males with autistic disorderI L Cohen, P M Vietze, V Sudhalter, et al.
American Journal of Medical Genetics|February 1, 1991
Detection of fragile X non-penetrant males by DNA marker analysisW T Brown, A Gross, P Goonewardena, et al.
American Journal of Medical Genetics|January 1, 1986
Variability of thymidylate synthase activity in whole blood cultures treated with FUdRS L Sklower, E C Jenkins, M L Anderson, et al.
American Journal of Medical Genetics|February 1, 1991
Cytogenetically negative, linkage positive "fragile X" syndromeS Sklower Brooks, I Cohen, C Ferrando, et al.
Human Genetics|June 30, 1977
De novo trisomy 9pter leads to q13N B Kardon, H R Salwen, M A Krauss, et al.
Lancet (London, England)|May 28, 1983
Testicular size in fetal fragile X syndromeR D Rudelli, E C Jenkins, K Wisniewski, et al.
American Journal of Medical Genetics|February 1, 1991
Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8W T Brown, A C Gross, P Goonewardena, et al.
Human Genetics|June 30, 1977
A case of 46,XY,t(1;13) (q24;q32) with mental retardationL Wilbur, F M Curcuru-Giordano, S G Krishna, et al.
Genetic Testing|September 12, 2001
PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensionsM Velinov, H Gu, K Shah, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|April 1, 1992
Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairmentW T Brown, E C Jenkins, P Goonewardena, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|November 1, 1989
Parent-child dyadic gaze patterns in fragile X males and in non-fragile X males with autistic disorderI L Cohen, P M Vietze, V Sudhalter, et al.
American Journal of Medical Genetics|February 1, 1991
Detection of fragile X non-penetrant males by DNA marker analysisW T Brown, A Gross, P Goonewardena, et al.
American Journal of Medical Genetics|January 1, 1986
Variability of thymidylate synthase activity in whole blood cultures treated with FUdRS L Sklower, E C Jenkins, M L Anderson, et al.
American Journal of Medical Genetics|February 1, 1991
Cytogenetically negative, linkage positive "fragile X" syndromeS Sklower Brooks, I Cohen, C Ferrando, et al.
Human Genetics|June 30, 1977
De novo trisomy 9pter leads to q13N B Kardon, H R Salwen, M A Krauss, et al.
Lancet (London, England)|May 28, 1983
Testicular size in fetal fragile X syndromeR D Rudelli, E C Jenkins, K Wisniewski, et al.
American Journal of Medical Genetics|February 1, 1991
Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8W T Brown, A C Gross, P Goonewardena, et al.
Human Genetics|June 30, 1977
A case of 46,XY,t(1;13) (q24;q32) with mental retardationL Wilbur, F M Curcuru-Giordano, S G Krishna, et al.
Genetic Testing|September 12, 2001
PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensionsM Velinov, H Gu, K Shah, et al.
Pageof 15