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I T Thomas

Showing results (21-30 of 30) with videos related to

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American Journal of Medical Genetics|February 1, 1987
Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiencyD S Rosenblatt, I T Thomas, D Watkins, et al.
American Journal of Medical Genetics|December 1, 1993
Najjar syndrome revisitedI T Thomas, T Jewett, P Lantz, et al.
American Journal of Medical Genetics|March 1, 1993
Inversion (X)(p11.4q22) associated with Norrie disease in a four generation familyM J Pettenati, P N Rao, R G Weaver, et al.
Human Genetics|August 1, 1992
Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardationM J Pettenati, N Rao, C Johnson, et al.
American Journal of Medical Genetics|December 1, 1993
Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23T Jewett, P N Rao, R G Weaver, et al.
Skeletal Radiology|January 1, 1991
Radiographic features of craniometadiaphyseal dysplasia, wormian bone typeL O Langer, P W Brill, E Afshani, et al.
American Journal of Medical Genetics|September 1, 1986
Isolated and syndromic cryptophthalmosI T Thomas, J L Frias, V Felix, et al.
American Journal of Human Genetics|August 1, 1989
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerismI T Thomas, J L Frias, E S Cantu, et al.
American Journal of Medical Genetics|February 1, 1993
Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two casesM J Pettenati, L A Teot, C Smith, et al.
American Journal of Human Genetics|May 29, 2000
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosomeM E Hodes, K Woodward, N B Spinner, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
American Journal of Medical Genetics|February 1, 1987
Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiencyD S Rosenblatt, I T Thomas, D Watkins, et al.
American Journal of Medical Genetics|December 1, 1993
Najjar syndrome revisitedI T Thomas, T Jewett, P Lantz, et al.
American Journal of Medical Genetics|March 1, 1993
Inversion (X)(p11.4q22) associated with Norrie disease in a four generation familyM J Pettenati, P N Rao, R G Weaver, et al.
Human Genetics|August 1, 1992
Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardationM J Pettenati, N Rao, C Johnson, et al.
American Journal of Medical Genetics|December 1, 1993
Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23T Jewett, P N Rao, R G Weaver, et al.
Skeletal Radiology|January 1, 1991
Radiographic features of craniometadiaphyseal dysplasia, wormian bone typeL O Langer, P W Brill, E Afshani, et al.
American Journal of Medical Genetics|September 1, 1986
Isolated and syndromic cryptophthalmosI T Thomas, J L Frias, V Felix, et al.
American Journal of Human Genetics|August 1, 1989
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerismI T Thomas, J L Frias, E S Cantu, et al.
American Journal of Medical Genetics|February 1, 1993
Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two casesM J Pettenati, L A Teot, C Smith, et al.
American Journal of Human Genetics|May 29, 2000
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosomeM E Hodes, K Woodward, N B Spinner, et al.
Pageof 3