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Clinical Genetics
|
November 1, 1984
Familial 5p- syndrome
T Kushnick, K W Rao, A N Lamb
American Journal of Obstetrics and Gynecology
|
October 20, 2001
Prenatal diagnosis from cystic hygroma fluid: the value of fluorescence in situ hybridization
A E Donnenfeld, D Lockwood, A N Lamb
Prenatal Diagnosis
|
April 24, 1999
Overwhelming maternal cell contamination in amniotic fluid samples from patients with oligohydramnios can lead to false prenatal interphase FISH results
L L Estabrooks, J S Hanna, A N Lamb
Molecular Biology and Evolution
|
March 1, 1987
Phylogenetic screening of the human genome: identification of differentially hybridizing repetitive sequence families
J A Lloyd, A N Lamb, S S Potter
American Journal of Medical Genetics
|
December 10, 1999
Autosomal XX sex reversal caused by duplication of SOX9
B Huang, S Wang, Y Ning, et al.
American Journal of Human Genetics
|
November 1, 1992
A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype
L L Estabrooks, A N Lamb, H N Kirkman, et al.
Journal of Medical Genetics
|
February 1, 1994
Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome
L L Estabrooks, A N Lamb, A S Aylsworth, et al.
Clinical Genetics
|
February 6, 2018
Prenatal detection of uniparental disomy of chromosome 2 carrying a CHRND pathogenic variant that causes lethal multiple pterygium syndrome
W Shen, B A Young, M Bosworth, et al.
American Journal of Medical Genetics
|
December 18, 1998
Identification of an unusual marker chromosome by spectral karyotyping
B Huang, Y Ning, A N Lamb, et al.
Human Reproduction (Oxford, England)
|
March 25, 1998
Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis
A M Estop, S Munné, K M Cieply, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Clinical Genetics
|
November 1, 1984
Familial 5p- syndrome
T Kushnick, K W Rao, A N Lamb
American Journal of Obstetrics and Gynecology
|
October 20, 2001
Prenatal diagnosis from cystic hygroma fluid: the value of fluorescence in situ hybridization
A E Donnenfeld, D Lockwood, A N Lamb
Prenatal Diagnosis
|
April 24, 1999
Overwhelming maternal cell contamination in amniotic fluid samples from patients with oligohydramnios can lead to false prenatal interphase FISH results
L L Estabrooks, J S Hanna, A N Lamb
Molecular Biology and Evolution
|
March 1, 1987
Phylogenetic screening of the human genome: identification of differentially hybridizing repetitive sequence families
J A Lloyd, A N Lamb, S S Potter
American Journal of Medical Genetics
|
December 10, 1999
Autosomal XX sex reversal caused by duplication of SOX9
B Huang, S Wang, Y Ning, et al.
American Journal of Human Genetics
|
November 1, 1992
A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype
L L Estabrooks, A N Lamb, H N Kirkman, et al.
Journal of Medical Genetics
|
February 1, 1994
Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome
L L Estabrooks, A N Lamb, A S Aylsworth, et al.
Clinical Genetics
|
February 6, 2018
Prenatal detection of uniparental disomy of chromosome 2 carrying a CHRND pathogenic variant that causes lethal multiple pterygium syndrome
W Shen, B A Young, M Bosworth, et al.
American Journal of Medical Genetics
|
December 18, 1998
Identification of an unusual marker chromosome by spectral karyotyping
B Huang, Y Ning, A N Lamb, et al.
Human Reproduction (Oxford, England)
|
March 25, 1998
Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis
A M Estop, S Munné, K M Cieply, et al.
Page
of 2