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Immunogenetics
|
January 1, 1989
The polymorphic Fc gamma receptor II gene maps to human chromosome 1q
H O Grundy, G Peltz, K W Moore, et al.
The Journal of Experimental Medicine
|
April 1, 1992
Localization of major histocompatibility complex class I and II mRNA in human first-trimester chorionic villi by in situ hybridization
J A Lata, R S Tuan, K J Shepley, et al.
American Journal of Medical Genetics
|
October 23, 1997
Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome
C E Anderson, R Wallerstein, S T Zamerowski, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
A (1;7) translocation, balanced, from a subject associated with repeated abortion. Respository identification No. GM-1356
L G Jackson, M F Sherwood, R C Miller, et al.
The New England Journal of Medicine
|
February 14, 1985
Prenatal diagnosis of Zellweger cerebrohepatorenal syndrome
A K Hajra, N S Datta, L G Jackson, et al.
American Journal of Human Genetics
|
April 1, 1986
Two abnormalities of hexosaminidase A in clinically normal individuals
E E Grebner, D A Mansfield, S S Raghavan, et al.
Nature
|
August 2, 1984
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients
T P Yang, P I Patel, A C Chinault, et al.
Lancet (London, England)
|
January 13, 1990
Selective reduction of multifetal pregnancies
R J Wapner, G H Davis, A Johnson, et al.
Prenatal Diagnosis
|
October 16, 1999
Fetal cells in maternal blood: NIFTY clinical trial interim analysis. DM-STAT. NICHD fetal cell study (NIFTY) group
D W Bianchi, J L Simpson, L G Jackson, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
June 2, 2001
Extra structurally abnormal chromosomes (ESACs)--presentation of 10 new cases
B Kałuzewski, Z Helszer, M Constantinou, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Immunogenetics
|
January 1, 1989
The polymorphic Fc gamma receptor II gene maps to human chromosome 1q
H O Grundy, G Peltz, K W Moore, et al.
The Journal of Experimental Medicine
|
April 1, 1992
Localization of major histocompatibility complex class I and II mRNA in human first-trimester chorionic villi by in situ hybridization
J A Lata, R S Tuan, K J Shepley, et al.
American Journal of Medical Genetics
|
October 23, 1997
Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome
C E Anderson, R Wallerstein, S T Zamerowski, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
A (1;7) translocation, balanced, from a subject associated with repeated abortion. Respository identification No. GM-1356
L G Jackson, M F Sherwood, R C Miller, et al.
The New England Journal of Medicine
|
February 14, 1985
Prenatal diagnosis of Zellweger cerebrohepatorenal syndrome
A K Hajra, N S Datta, L G Jackson, et al.
American Journal of Human Genetics
|
April 1, 1986
Two abnormalities of hexosaminidase A in clinically normal individuals
E E Grebner, D A Mansfield, S S Raghavan, et al.
Nature
|
August 2, 1984
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients
T P Yang, P I Patel, A C Chinault, et al.
Lancet (London, England)
|
January 13, 1990
Selective reduction of multifetal pregnancies
R J Wapner, G H Davis, A Johnson, et al.
Prenatal Diagnosis
|
October 16, 1999
Fetal cells in maternal blood: NIFTY clinical trial interim analysis. DM-STAT. NICHD fetal cell study (NIFTY) group
D W Bianchi, J L Simpson, L G Jackson, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
June 2, 2001
Extra structurally abnormal chromosomes (ESACs)--presentation of 10 new cases
B Kałuzewski, Z Helszer, M Constantinou, et al.
Page
of 8