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M Bobrow

Showing results (141-150 of 235) with videos related to

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The Journal of Pediatrics|February 1, 1973
Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndromeK Taysi, M Bobrow, S Balci, et al.
Annals of Human Genetics|July 1, 1974
Probable assignment of the locus determining human red cell acid phosphatase ACP1 to chromosome 2 using somatic cell hybridsS Povey, D M Swallow, M Bobrow, et al.
Human Mutation|January 1, 1995
Detection of 12 novel mutations in the collagenous domain of the COL4A5 gene in Alport syndrome patientsE Boye, F Flinter, J Zhou, et al.
Journal of Medical Screening|October 1, 1994
Monitoring trends in prenatal diagnosis of Down's syndrome in England and Wales, 1989-92J K Morris, D E Mutton, R Ide, et al.
Annals of the New York Academy of Sciences|September 7, 1994
An improved method for the detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridizationA F Davies, L Barber, M Murer-Orlando, et al.
Journal of Medical Genetics|September 1, 1994
FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigsA F Davies, L Barber, M Murer-Orlando, et al.
Lancet (London, England)|October 29, 1988
Genetics of classic Alport's syndromeF A Flinter, J S Cameron, C Chantler, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Regional mapping of chromosome 15L Pajunen, E Solomon, S Burgess, et al.
American Journal of Human Genetics|October 1, 1995
The natural history of Down syndrome conceptuses diagnosed prenatally that are not electively terminatedE B Hook, D E Mutton, R Ide, et al.
Birth Defects Original Article Series|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, et al.
Pageof 24

Showing results (141-150 of 235) with videos related to

Sort By:
Pageof 24
The Journal of Pediatrics|February 1, 1973
Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndromeK Taysi, M Bobrow, S Balci, et al.
Annals of Human Genetics|July 1, 1974
Probable assignment of the locus determining human red cell acid phosphatase ACP1 to chromosome 2 using somatic cell hybridsS Povey, D M Swallow, M Bobrow, et al.
Human Mutation|January 1, 1995
Detection of 12 novel mutations in the collagenous domain of the COL4A5 gene in Alport syndrome patientsE Boye, F Flinter, J Zhou, et al.
Journal of Medical Screening|October 1, 1994
Monitoring trends in prenatal diagnosis of Down's syndrome in England and Wales, 1989-92J K Morris, D E Mutton, R Ide, et al.
Annals of the New York Academy of Sciences|September 7, 1994
An improved method for the detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridizationA F Davies, L Barber, M Murer-Orlando, et al.
Journal of Medical Genetics|September 1, 1994
FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigsA F Davies, L Barber, M Murer-Orlando, et al.
Lancet (London, England)|October 29, 1988
Genetics of classic Alport's syndromeF A Flinter, J S Cameron, C Chantler, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Regional mapping of chromosome 15L Pajunen, E Solomon, S Burgess, et al.
American Journal of Human Genetics|October 1, 1995
The natural history of Down syndrome conceptuses diagnosed prenatally that are not electively terminatedE B Hook, D E Mutton, R Ide, et al.
Birth Defects Original Article Series|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, et al.
Pageof 24