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Human Reproduction (Oxford, England)
|
December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British survey
A G Sutcliffe, C J Peters, S Bowdin, et al.
Genomics
|
December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11
R J Smith, E C Lee, W J Kimberling, et al.
American Journal of Human Genetics
|
June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy
H G Harley, S A Rundle, J C MacMillan, et al.
European Journal of Pediatrics
|
December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two families
J Wang, L Spitz, R Hayward, et al.
Genomics
|
December 1, 1992
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
W J Kimberling, C G Möller, S Davenport, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus
L J Pulleyn, W Reardon, D Wilkes, et al.
American Journal of Human Genetics
|
July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)
I Bach, H G Brunner, P Beighton, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
February 17, 2005
Outbreak of listeriosis among Mexican immigrants as a result of consumption of illicitly produced Mexican-style cheese
Pia D M MacDonald, Robert E Whitwam, Jackie D Boggs, et al.
Journal of Medical Genetics
|
January 3, 2001
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss
M J Houseman, L A Ellis, A Pagnamenta, et al.
Journal of Medical Genetics
|
August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis
W Reardon, D Wilkes, P Rutland, et al.
Page
of 17
Search research articles
Search
Showing results (131-140 of 166) with videos related to
Sort By:
Page
of 17
Human Reproduction (Oxford, England)
|
December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British survey
A G Sutcliffe, C J Peters, S Bowdin, et al.
Genomics
|
December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11
R J Smith, E C Lee, W J Kimberling, et al.
American Journal of Human Genetics
|
June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy
H G Harley, S A Rundle, J C MacMillan, et al.
European Journal of Pediatrics
|
December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two families
J Wang, L Spitz, R Hayward, et al.
Genomics
|
December 1, 1992
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
W J Kimberling, C G Möller, S Davenport, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus
L J Pulleyn, W Reardon, D Wilkes, et al.
American Journal of Human Genetics
|
July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)
I Bach, H G Brunner, P Beighton, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
February 17, 2005
Outbreak of listeriosis among Mexican immigrants as a result of consumption of illicitly produced Mexican-style cheese
Pia D M MacDonald, Robert E Whitwam, Jackie D Boggs, et al.
Journal of Medical Genetics
|
January 3, 2001
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss
M J Houseman, L A Ellis, A Pagnamenta, et al.
Journal of Medical Genetics
|
August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis
W Reardon, D Wilkes, P Rutland, et al.
Page
of 17