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L L Field

Showing results (41-50 of 59) with videos related to

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Human Heredity|January 1, 1985
Glutamate pyruvate transaminase null allele (GPT0) in the NavajoM Crist, J R Heckenlively, L L Field, et al.
Human Heredity|January 1, 1984
Genetic linkage studies of transferrin, pseudocholinesterase, and chromosome 1 lociR S Sparkes, L L Field, M C Sparkes, et al.
Human Genetics|September 1, 1989
Mapping studies of the serum cholinesterase-2 locus (CHE2)M L Marazita, B J Keats, M A Spence, et al.
Science (New York, N.Y.)|February 25, 1983
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase DR S Sparkes, A L Murphree, R W Lingua, et al.
American Journal of Medical Genetics|August 10, 2001
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexiaT L Petryshen, B J Kaplan, M Fu Liu, et al.
Human Genetics|April 1, 1990
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeN T Bech-Hansen, L L Field, A M Schramm, et al.
American Journal of Human Genetics|October 27, 1997
Association mapping of disease loci, by use of a pooled DNA genomic screenL F Barcellos, W Klitz, L L Field, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1983
Genetic linkage studies with cleft lip and palate: report of two family studiesM A Spence, L Glass, B F Crandall, et al.
Clinical Genetics|August 25, 2004
TP63 mutation and clefting modifier genes in an EEC syndrome familyA K Ray, M L Marazita, R Pathak, et al.
Journal of Medical Genetics|October 1, 1983
Linkage analysis of neurofibromatosis (von Recklinghausen disease)M A Spence, J L Bader, D M Parry, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Human Heredity|January 1, 1985
Glutamate pyruvate transaminase null allele (GPT0) in the NavajoM Crist, J R Heckenlively, L L Field, et al.
Human Heredity|January 1, 1984
Genetic linkage studies of transferrin, pseudocholinesterase, and chromosome 1 lociR S Sparkes, L L Field, M C Sparkes, et al.
Human Genetics|September 1, 1989
Mapping studies of the serum cholinesterase-2 locus (CHE2)M L Marazita, B J Keats, M A Spence, et al.
Science (New York, N.Y.)|February 25, 1983
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase DR S Sparkes, A L Murphree, R W Lingua, et al.
American Journal of Medical Genetics|August 10, 2001
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexiaT L Petryshen, B J Kaplan, M Fu Liu, et al.
Human Genetics|April 1, 1990
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeN T Bech-Hansen, L L Field, A M Schramm, et al.
American Journal of Human Genetics|October 27, 1997
Association mapping of disease loci, by use of a pooled DNA genomic screenL F Barcellos, W Klitz, L L Field, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1983
Genetic linkage studies with cleft lip and palate: report of two family studiesM A Spence, L Glass, B F Crandall, et al.
Clinical Genetics|August 25, 2004
TP63 mutation and clefting modifier genes in an EEC syndrome familyA K Ray, M L Marazita, R Pathak, et al.
Journal of Medical Genetics|October 1, 1983
Linkage analysis of neurofibromatosis (von Recklinghausen disease)M A Spence, J L Bader, D M Parry, et al.
Pageof 6