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B Say

Showing results (111-120 of 141) with videos related to

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American Journal of Medical Genetics|March 13, 1995
CD1+ cells in mothers of stillborn infants with neural tube defectsF N Seniz, E Müftüoğlu, M S Batun, et al.
Pediatric Radiology|July 1, 1973
Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: a case reportB Say, S Balci, T Pirnar, et al.
The Journal of the Oklahoma State Medical Association|March 21, 1998
Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosisB Can, F V Schaefer, S Malik, et al.
Clinical Nuclear Medicine|August 17, 2001
Diagnosis of brain infarction on lung perfusion scintigraphyM Onur Demirkol, B Mutlu, B Say, et al.
Clinical Genetics|November 27, 1998
Two sisters with different chromosomal microdeletions: Rubinstein-Taybi syndrome and 22q deletion syndromeB Can, Y Qu, L G Jackson, et al.
Journal of Medical Genetics|October 1, 1980
The Gordon syndromeB Say, D H Barber, R C Thompson, et al.
Birth Defects Original Article Series|January 1, 1976
Polydactyly with triphalangeal thumbs, brachydactyly, camptodactyly, congenital dislocation of the patellas, short stature and borderline intelligenceB Say, E Feild, J G Coldwell, et al.
The Journal of Pediatrics|March 1, 1976
Familial translocation (3p 15p) with partial trisomy for the upper arm of chromosome 3 in two sibsB Say, N Barber, M Bobrow, et al.
Journal of Medical Genetics|November 1, 1987
Partial deletion 21: case report with biochemical studies and reviewN J Carpenter, J S Mayes, B Say, et al.
Journal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|March 13, 1995
CD1+ cells in mothers of stillborn infants with neural tube defectsF N Seniz, E Müftüoğlu, M S Batun, et al.
Pediatric Radiology|July 1, 1973
Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: a case reportB Say, S Balci, T Pirnar, et al.
The Journal of the Oklahoma State Medical Association|March 21, 1998
Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosisB Can, F V Schaefer, S Malik, et al.
Clinical Nuclear Medicine|August 17, 2001
Diagnosis of brain infarction on lung perfusion scintigraphyM Onur Demirkol, B Mutlu, B Say, et al.
Clinical Genetics|November 27, 1998
Two sisters with different chromosomal microdeletions: Rubinstein-Taybi syndrome and 22q deletion syndromeB Can, Y Qu, L G Jackson, et al.
Journal of Medical Genetics|October 1, 1980
The Gordon syndromeB Say, D H Barber, R C Thompson, et al.
Birth Defects Original Article Series|January 1, 1976
Polydactyly with triphalangeal thumbs, brachydactyly, camptodactyly, congenital dislocation of the patellas, short stature and borderline intelligenceB Say, E Feild, J G Coldwell, et al.
The Journal of Pediatrics|March 1, 1976
Familial translocation (3p 15p) with partial trisomy for the upper arm of chromosome 3 in two sibsB Say, N Barber, M Bobrow, et al.
Journal of Medical Genetics|November 1, 1987
Partial deletion 21: case report with biochemical studies and reviewN J Carpenter, J S Mayes, B Say, et al.
Journal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.
Pageof 15