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Southern Medical Journal
|
March 1, 1995
Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992
M G Butler, T Hamill
Journal of the American Academy of Dermatology
|
July 1, 1989
Urticaria pigmentosa in a child with Prader-Labhart-Willi syndrome
J F Fowler, M G Butler
Lancet (London, England)
|
June 4, 1983
Parental origin of chromosome 15 deletion in Prader-Willi syndrome
M G Butler, C G Palmer
American Journal of Medical Genetics
|
August 1, 1986
Metacarpophalangeal pattern profile analysis in Sotos syndrome: an update
M G Butler, F J Meaney
Mechanisms of Ageing and Development
|
January 1, 1989
Effects of age, sex and multiple endocrine neoplasia type-II on silver stained nucleolar organizer regions
M G Butler, J R Lane
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
December 1, 1995
Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases
R S Larson, M G Butler
American Journal of Medical Genetics
|
December 1, 1988
Do some patients with fragile X syndrome have precocious puberty?
M G Butler, J L Najjar
American Journal of Physical Anthropology
|
December 1, 1987
Craniofacial variation and growth in the Prader-Labhart-Willi syndrome
F J Meaney, M G Butler
Journal of Clinical Epigenetics
|
January 24, 2017
Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi Syndrome
A M Manzardo, M G Butler
The International Journal of Pediatric Nephrology
|
October 1, 1987
Renal and urinary tract abnormalities associated with chromosome aberrations
A Y Barakat, M G Butler
Page
of 22
Search research articles
Search
Showing results (21-30 of 212) with videos related to
Sort By:
Page
of 22
Southern Medical Journal
|
March 1, 1995
Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992
M G Butler, T Hamill
Journal of the American Academy of Dermatology
|
July 1, 1989
Urticaria pigmentosa in a child with Prader-Labhart-Willi syndrome
J F Fowler, M G Butler
Lancet (London, England)
|
June 4, 1983
Parental origin of chromosome 15 deletion in Prader-Willi syndrome
M G Butler, C G Palmer
American Journal of Medical Genetics
|
August 1, 1986
Metacarpophalangeal pattern profile analysis in Sotos syndrome: an update
M G Butler, F J Meaney
Mechanisms of Ageing and Development
|
January 1, 1989
Effects of age, sex and multiple endocrine neoplasia type-II on silver stained nucleolar organizer regions
M G Butler, J R Lane
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
December 1, 1995
Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases
R S Larson, M G Butler
American Journal of Medical Genetics
|
December 1, 1988
Do some patients with fragile X syndrome have precocious puberty?
M G Butler, J L Najjar
American Journal of Physical Anthropology
|
December 1, 1987
Craniofacial variation and growth in the Prader-Labhart-Willi syndrome
F J Meaney, M G Butler
Journal of Clinical Epigenetics
|
January 24, 2017
Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi Syndrome
A M Manzardo, M G Butler
The International Journal of Pediatric Nephrology
|
October 1, 1987
Renal and urinary tract abnormalities associated with chromosome aberrations
A Y Barakat, M G Butler
Page
of 22