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American Journal of Medical Genetics
|
December 2, 1996
Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion
M Clemens, J T Martsolf, J G Rogers, et al.
American Journal of Medical Genetics
|
December 23, 1999
Mosaicism in Prader-Willi syndrome
P A Mowery-Rushton, J M Hanchett, W B Zipf, et al.
American Journal of Obstetrics and Gynecology
|
May 15, 1984
Human chorionic gonadotropin levels in complete and partial hydatidiform moles and in nonmolar abortuses
E B Smith, A E Szulman, W Hinshaw, et al.
Cancer Genetics and Cytogenetics
|
May 1, 1993
Cytogenetic findings in a symplastic leiomyoma
Y Y Ozisik, A M Meloni, A A Sandberg, et al.
American Journal of Human Genetics
|
May 10, 2000
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole
M V Zaragoza, U Surti, R W Redline, et al.
Nature Genetics
|
November 1, 1994
Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype
B T Lahn, N Ma, W R Breg, et al.
American Journal of Human Genetics
|
July 1, 1994
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations
D J Wolff, C J Brown, S Schwartz, et al.
Journal of Pediatric Hematology/Oncology
|
April 17, 1998
Nongestational choriocarcinoma in the postpartum period: a case report
K Suryanarayan, K A O'Hanlan, U Surti, et al.
Genes, Chromosomes & Cancer
|
September 1, 1995
Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas
C S Ishwad, R E Ferrell, J Davare, et al.
American Journal of Human Genetics
|
October 1, 1990
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers
R Deka, A Chakravarti, U Surti, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 89) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics
|
December 2, 1996
Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion
M Clemens, J T Martsolf, J G Rogers, et al.
American Journal of Medical Genetics
|
December 23, 1999
Mosaicism in Prader-Willi syndrome
P A Mowery-Rushton, J M Hanchett, W B Zipf, et al.
American Journal of Obstetrics and Gynecology
|
May 15, 1984
Human chorionic gonadotropin levels in complete and partial hydatidiform moles and in nonmolar abortuses
E B Smith, A E Szulman, W Hinshaw, et al.
Cancer Genetics and Cytogenetics
|
May 1, 1993
Cytogenetic findings in a symplastic leiomyoma
Y Y Ozisik, A M Meloni, A A Sandberg, et al.
American Journal of Human Genetics
|
May 10, 2000
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole
M V Zaragoza, U Surti, R W Redline, et al.
Nature Genetics
|
November 1, 1994
Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype
B T Lahn, N Ma, W R Breg, et al.
American Journal of Human Genetics
|
July 1, 1994
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations
D J Wolff, C J Brown, S Schwartz, et al.
Journal of Pediatric Hematology/Oncology
|
April 17, 1998
Nongestational choriocarcinoma in the postpartum period: a case report
K Suryanarayan, K A O'Hanlan, U Surti, et al.
Genes, Chromosomes & Cancer
|
September 1, 1995
Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas
C S Ishwad, R E Ferrell, J Davare, et al.
American Journal of Human Genetics
|
October 1, 1990
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers
R Deka, A Chakravarti, U Surti, et al.
Page
of 9