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R L Neu

Showing results (51-60 of 58) with videos related to

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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.
American Journal of Diseases of Children (1960)|October 1, 1979
Family with three apparently balanced t(3;15) (p27;q22) translocation carriers. Association with deficits in language acquisition and mental retardation: a possible example of position effect in manL I Gardner, R L Neu, R S Shah, et al.
Journal of Medical Genetics|December 1, 1976
Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18R L Neu, C C Ortega, G A Barg, et al.
Journal of Medical Genetics|September 1, 1988
Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parentsR L Neu, B G Kousseff, D E Hardy, et al.
American Journal of Medical Genetics|February 7, 1998
Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatinP Ashton-Prolla, I F Gershin, A Babu, et al.
Journal of Medical Genetics|December 1, 1987
Ultrasound identification of apparently normal male genitalia in a 46,X,+mar fetusR L Neu, W F O'Brien, B G Kousseff, et al.
Prenatal Diagnosis|March 1, 1997
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlationsL Y Hsu, M T Yu, R L Neu, et al.
Prenatal Diagnosis|March 1, 2000
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlationsR Wallerstein, M T Yu, R L Neu, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
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.
American Journal of Diseases of Children (1960)|October 1, 1979
Family with three apparently balanced t(3;15) (p27;q22) translocation carriers. Association with deficits in language acquisition and mental retardation: a possible example of position effect in manL I Gardner, R L Neu, R S Shah, et al.
Journal of Medical Genetics|December 1, 1976
Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18R L Neu, C C Ortega, G A Barg, et al.
Journal of Medical Genetics|September 1, 1988
Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parentsR L Neu, B G Kousseff, D E Hardy, et al.
American Journal of Medical Genetics|February 7, 1998
Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatinP Ashton-Prolla, I F Gershin, A Babu, et al.
Journal of Medical Genetics|December 1, 1987
Ultrasound identification of apparently normal male genitalia in a 46,X,+mar fetusR L Neu, W F O'Brien, B G Kousseff, et al.
Prenatal Diagnosis|March 1, 1997
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlationsL Y Hsu, M T Yu, R L Neu, et al.
Prenatal Diagnosis|March 1, 2000
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlationsR Wallerstein, M T Yu, R L Neu, et al.
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