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M G Butler

Showing results (191-200 of 212) with videos related to

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Clinical Dysmorphology|April 20, 2001
Total anomalous pulmonary venous connection and a constellation of craniofacial, skeletal, and urogenital anomalies in a newborn and similar features in his 36-year-old fatherD M Pierson, E M Taboada, G K Lofland, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Pediatrics|February 1, 1993
Prader-Willi syndrome: consensus diagnostic criteriaV A Holm, S B Cassidy, M G Butler, et al.
Chest|June 1, 1997
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansionJ E Loyd, B Slovis, J A Phillips, et al.
American Journal of Medical Genetics|March 21, 1998
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7qG H Vance, C Nickerson, L Sarnat, et al.
Genome|November 18, 2000
Intercontinental karyotypic differentiation of Chironomus entis Shobanov, a Holarctic member of the C. plumosus group (Diptera, Chironomidae)I I Kiknadze, M G Butler, V V Golygina, et al.
Fertility and Sterility|October 1, 1986
A child with 45,X/46,X,del(Y)(q12) identified with a Y-specific probeM G Butler, V G Dev, J A Phillips, et al.
Histopathology|November 1, 1986
Cytokeratin and laminin immunostaining in the diagnosis of cutaneous neuro-endocrine (Merkel cell) tumoursP A Hall, A J d'Ardenne, M G Butler, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics ProgramG W Dewald, A R Brothman, M G Butler, et al.
American Journal of Medical Genetics|March 1, 1996
Distinct 15q genotypes in Russell-Silver and ring 15 syndromesP K Rogan, J R Seip, D J Driscoll, et al.
Pageof 22

Showing results (191-200 of 212) with videos related to

Sort By:
Pageof 22
Clinical Dysmorphology|April 20, 2001
Total anomalous pulmonary venous connection and a constellation of craniofacial, skeletal, and urogenital anomalies in a newborn and similar features in his 36-year-old fatherD M Pierson, E M Taboada, G K Lofland, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Pediatrics|February 1, 1993
Prader-Willi syndrome: consensus diagnostic criteriaV A Holm, S B Cassidy, M G Butler, et al.
Chest|June 1, 1997
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansionJ E Loyd, B Slovis, J A Phillips, et al.
American Journal of Medical Genetics|March 21, 1998
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7qG H Vance, C Nickerson, L Sarnat, et al.
Genome|November 18, 2000
Intercontinental karyotypic differentiation of Chironomus entis Shobanov, a Holarctic member of the C. plumosus group (Diptera, Chironomidae)I I Kiknadze, M G Butler, V V Golygina, et al.
Fertility and Sterility|October 1, 1986
A child with 45,X/46,X,del(Y)(q12) identified with a Y-specific probeM G Butler, V G Dev, J A Phillips, et al.
Histopathology|November 1, 1986
Cytokeratin and laminin immunostaining in the diagnosis of cutaneous neuro-endocrine (Merkel cell) tumoursP A Hall, A J d'Ardenne, M G Butler, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics ProgramG W Dewald, A R Brothman, M G Butler, et al.
American Journal of Medical Genetics|March 1, 1996
Distinct 15q genotypes in Russell-Silver and ring 15 syndromesP K Rogan, J R Seip, D J Driscoll, et al.
Pageof 22