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Journal of Medical Genetics
|
February 1, 1994
Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome
B Z Garty, B Eisenstein, J Sandbank, et al.
American Journal of Medical Genetics
|
July 27, 2001
Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4
P D Cotter, S Kaffe, L Li, et al.
American Journal of Ophthalmology
|
September 1, 1982
Autosomal dominant inheritance of retinoschisis
Y Yassur, I Nissenkorn, I Ben-Sira, et al.
Journal of Medical Genetics
|
December 1, 1977
Supernumerary small ring chromosome
S Kaffe, H J Kim, L Y Hsu, et al.
Nature
|
January 27, 1983
U cells contain contaminants
W C Wright, S Kaffe, C F Holinka, et al.
Prenatal Diagnosis
|
December 1, 1989
A rare case of 68,XX triploidy diagnosed by amniocentesis
S Kaffe, C Eliasen, L Wan, et al.
American Journal of Medical Genetics
|
May 2, 1997
Paternal uniparental disomy for chromosome 14: a case report and review
P D Cotter, S Kaffe, L D McCurdy, et al.
American Journal of Medical Genetics
|
January 1, 1977
Prenatal diagnosis of renal anomalies
S Kaffe, J S Rose, L Godmilow, et al.
American Journal of Medical Genetics
|
January 1, 1978
Prenatal cytogenetic diagnosis: first 1,000 successful cases
L Y Hsu, S Kaffe, F Yahr, et al.
Prenatal Diagnosis
|
July 1, 1992
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
L Y Hsu, S Kaffe, E C Jenkins, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Journal of Medical Genetics
|
February 1, 1994
Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome
B Z Garty, B Eisenstein, J Sandbank, et al.
American Journal of Medical Genetics
|
July 27, 2001
Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4
P D Cotter, S Kaffe, L Li, et al.
American Journal of Ophthalmology
|
September 1, 1982
Autosomal dominant inheritance of retinoschisis
Y Yassur, I Nissenkorn, I Ben-Sira, et al.
Journal of Medical Genetics
|
December 1, 1977
Supernumerary small ring chromosome
S Kaffe, H J Kim, L Y Hsu, et al.
Nature
|
January 27, 1983
U cells contain contaminants
W C Wright, S Kaffe, C F Holinka, et al.
Prenatal Diagnosis
|
December 1, 1989
A rare case of 68,XX triploidy diagnosed by amniocentesis
S Kaffe, C Eliasen, L Wan, et al.
American Journal of Medical Genetics
|
May 2, 1997
Paternal uniparental disomy for chromosome 14: a case report and review
P D Cotter, S Kaffe, L D McCurdy, et al.
American Journal of Medical Genetics
|
January 1, 1977
Prenatal diagnosis of renal anomalies
S Kaffe, J S Rose, L Godmilow, et al.
American Journal of Medical Genetics
|
January 1, 1978
Prenatal cytogenetic diagnosis: first 1,000 successful cases
L Y Hsu, S Kaffe, F Yahr, et al.
Prenatal Diagnosis
|
July 1, 1992
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
L Y Hsu, S Kaffe, E C Jenkins, et al.
Page
of 4