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Investigative Ophthalmology & Visual Science
|
March 11, 2000
Adenovirus keratitis: a role for interleukin-8
J Chodosh, R A Astley, M G Butler, et al.
Child Nephrology and Urology
|
January 1, 1990
Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndrome
A J Barakat, P Arianas, A D Glick, et al.
American Journal of Medical Genetics
|
October 16, 1996
A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13
M G Butler, S L Christian, T Kubota, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1992
Cytogenetic abnormalities in a rare case of giant cell osteogenic sarcoma
H S Schwartz, G A Allen, I Chudoba, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1996
Chromosome telomere integrity of human solid neoplasms
M G Butler, M Sciadini, L K Hedges, et al.
American Journal of Medical Genetics
|
July 1, 1987
Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?
M G Butler, B D Hall, R N Maclean, et al.
Clinical Genetics
|
October 7, 2017
Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults
A M Manzardo, N Weisensel, S Ayala, et al.
American Journal of Medical Genetics
|
July 3, 1995
Identification of a ring chromosome as a ring 8 using fluorescent in situ hybridization (FISH) in a child with multiple congenital anomalies
M G Butler, E W Roback, G A Allen, et al.
American Journal of Medical Genetics
|
September 15, 1993
Metacarpophalangeal pattern profile analysis in Williams syndrome
M A Burns, D R McLeod, L R Linton, et al.
American Journal of Medical Genetics
|
January 1, 1988
Metacarpophalangeal pattern profile analysis in Sotos syndrome: a follow-up report on 34 subjects
M G Butler, P F Dijkstra, F J Meaney, et al.
Page
of 22
Search research articles
Search
Showing results (101-110 of 212) with videos related to
Sort By:
Page
of 22
Investigative Ophthalmology & Visual Science
|
March 11, 2000
Adenovirus keratitis: a role for interleukin-8
J Chodosh, R A Astley, M G Butler, et al.
Child Nephrology and Urology
|
January 1, 1990
Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndrome
A J Barakat, P Arianas, A D Glick, et al.
American Journal of Medical Genetics
|
October 16, 1996
A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13
M G Butler, S L Christian, T Kubota, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1992
Cytogenetic abnormalities in a rare case of giant cell osteogenic sarcoma
H S Schwartz, G A Allen, I Chudoba, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1996
Chromosome telomere integrity of human solid neoplasms
M G Butler, M Sciadini, L K Hedges, et al.
American Journal of Medical Genetics
|
July 1, 1987
Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?
M G Butler, B D Hall, R N Maclean, et al.
Clinical Genetics
|
October 7, 2017
Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults
A M Manzardo, N Weisensel, S Ayala, et al.
American Journal of Medical Genetics
|
July 3, 1995
Identification of a ring chromosome as a ring 8 using fluorescent in situ hybridization (FISH) in a child with multiple congenital anomalies
M G Butler, E W Roback, G A Allen, et al.
American Journal of Medical Genetics
|
September 15, 1993
Metacarpophalangeal pattern profile analysis in Williams syndrome
M A Burns, D R McLeod, L R Linton, et al.
American Journal of Medical Genetics
|
January 1, 1988
Metacarpophalangeal pattern profile analysis in Sotos syndrome: a follow-up report on 34 subjects
M G Butler, P F Dijkstra, F J Meaney, et al.
Page
of 22