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L Neu

Showing results (51-60 of 75) with videos related to

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Journal of Medical Genetics|August 1, 1976
46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiencyR L Neu, J A Stockman, R E Spitzer, et al.
Annales De Genetique|January 1, 1979
An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) motherR L Neu, N R Dennis, J T Lanman, et al.
Journal of Medical Genetics|March 1, 1970
A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-)G J Bargman, R L Neu, H O Powers, et al.
Journal of Medical Genetics|March 1, 1973
Three generations and six family members with a t(13q15q) chromosomeR L Neu, L I Gardner, M L Williams, et al.
Clinical Genetics|September 1, 1992
Cleft palate and complex chromosome rearrangementsB G Kousseff, P Papenhausen, R L Neu, et al.
Transplantation Proceedings|August 1, 1993
Improving renal transplant outcomes in African Americans with OKT3 induction therapyJ A Light, J L Kelly, A Aquino, et al.
Annales De Genetique|January 1, 1981
An infant with trisomy 6q21 leads to 6qterR L Neu, J U Gallien, N Steinberg-Warren, et al.
American Journal of Medical Genetics|January 1, 1981
Brief clinical report: an infant with duplication of 17q21 lead to 17qterJ U Gallien, R L Neu, R J Wynn, et al.
Ecology and Evolution|June 25, 2025
Effect of Food Mass in the Gut on the Metabolic Rate of <i>Carcinus maenas</i> in the FieldDavid L Neu, Laura S Fletcher, Mikayla Bolander, et al.
Clinical Genetics|February 1, 1988
Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomaliesR L Neu, B G Kousseff, S Madan, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|August 1, 1976
46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiencyR L Neu, J A Stockman, R E Spitzer, et al.
Annales De Genetique|January 1, 1979
An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) motherR L Neu, N R Dennis, J T Lanman, et al.
Journal of Medical Genetics|March 1, 1970
A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-)G J Bargman, R L Neu, H O Powers, et al.
Journal of Medical Genetics|March 1, 1973
Three generations and six family members with a t(13q15q) chromosomeR L Neu, L I Gardner, M L Williams, et al.
Clinical Genetics|September 1, 1992
Cleft palate and complex chromosome rearrangementsB G Kousseff, P Papenhausen, R L Neu, et al.
Transplantation Proceedings|August 1, 1993
Improving renal transplant outcomes in African Americans with OKT3 induction therapyJ A Light, J L Kelly, A Aquino, et al.
Annales De Genetique|January 1, 1981
An infant with trisomy 6q21 leads to 6qterR L Neu, J U Gallien, N Steinberg-Warren, et al.
American Journal of Medical Genetics|January 1, 1981
Brief clinical report: an infant with duplication of 17q21 lead to 17qterJ U Gallien, R L Neu, R J Wynn, et al.
Ecology and Evolution|June 25, 2025
Effect of Food Mass in the Gut on the Metabolic Rate of <i>Carcinus maenas</i> in the FieldDavid L Neu, Laura S Fletcher, Mikayla Bolander, et al.
Clinical Genetics|February 1, 1988
Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomaliesR L Neu, B G Kousseff, S Madan, et al.
Pageof 8