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American Journal of Human Genetics
|
April 1, 1997
Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction
W P Robinson, I J Barrett, L Bernard, et al.
American Journal of Medical Genetics
|
August 15, 1994
Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis
H Cole, B Huang, B A Salbert, et al.
American Journal of Medical Genetics
|
July 12, 1996
Molecular fragile X screening in normal populations
W C Spence, S H Black, L Fallon, et al.
American Journal of Medical Genetics
|
April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?
G S Fisch, L R Shapiro, R Simensen, et al.
Clinical Genetics
|
January 10, 2001
An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta
M S Peñaherrera, I J Barrett, C J Brown, et al.
American Journal of Medical Genetics
|
June 1, 1987
ReCAP: the Registry of Cytogenetic Abnormalities and Phenylketonuria
J M Friedman, J P Smith, B N Lerner, et al.
American Journal of Medical Genetics
|
February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter study
G S Fisch, T Arinami, U Froster-Iskenius, et al.
Human Genetics
|
January 1, 1985
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
S L Sherman, P A Jacobs, N E Morton, et al.
American Journal of Medical Genetics
|
February 1, 1991
Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures
E C Jenkins, M S Krawczun, S L Stark-Houck, et al.
American Journal of Human Genetics
|
March 21, 2000
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population
D C Crawford, C E Schwartz, K L Meadows, et al.
Page
of 10
Search research articles
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Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
April 1, 1997
Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction
W P Robinson, I J Barrett, L Bernard, et al.
American Journal of Medical Genetics
|
August 15, 1994
Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis
H Cole, B Huang, B A Salbert, et al.
American Journal of Medical Genetics
|
July 12, 1996
Molecular fragile X screening in normal populations
W C Spence, S H Black, L Fallon, et al.
American Journal of Medical Genetics
|
April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?
G S Fisch, L R Shapiro, R Simensen, et al.
Clinical Genetics
|
January 10, 2001
An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta
M S Peñaherrera, I J Barrett, C J Brown, et al.
American Journal of Medical Genetics
|
June 1, 1987
ReCAP: the Registry of Cytogenetic Abnormalities and Phenylketonuria
J M Friedman, J P Smith, B N Lerner, et al.
American Journal of Medical Genetics
|
February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter study
G S Fisch, T Arinami, U Froster-Iskenius, et al.
Human Genetics
|
January 1, 1985
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
S L Sherman, P A Jacobs, N E Morton, et al.
American Journal of Medical Genetics
|
February 1, 1991
Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures
E C Jenkins, M S Krawczun, S L Stark-Houck, et al.
American Journal of Human Genetics
|
March 21, 2000
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population
D C Crawford, C E Schwartz, K L Meadows, et al.
Page
of 10