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Journal of Molecular Evolution
|
August 1, 1991
Evolution and sequence analysis of a human Y-chromosomal DNA fragment
E C Whisenant, B K Rasheed, H Ostrer, et al.
The Journal of Pediatrics
|
June 1, 1989
Familial XX chromosomal maleness does not arise from a Y chromosomal translocation
H Ostrer, G Wright, M Clayton, et al.
Clinical Dysmorphology
|
November 21, 1998
Acro-renal-ocular syndrome: expansion of the phenotype
E Guillén-Navarro, R Wallerstein, E Reich, et al.
American Journal of Human Genetics
|
December 1, 1988
Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes
E S Cantú, R D Marsh, K E Boecklen, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
January 7, 1998
X-inactivation and cytogenetic studies in a family with sensorineural hearing loss and Turner syndrome
N Sculerati, M A Perle, C Oddoux, et al.
British Journal of Haematology
|
December 24, 1997
Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11
B Wistinghausen, A Reischer, C Oddoux, et al.
Clinical Genetics
|
April 16, 2003
Genetic counseling for prostate cancer risk
A M Nieder, S S Taneja, M P A Zeegers, et al.
Experimental Cell Research
|
June 1, 1986
Human histone gene organization. Identification of a histone gene polymorphism prevalent in a black population
L Green, W Whittle, R Dell'Orco, et al.
JAMA
|
March 4, 1992
Genetic screening by insurance carriers
M A Dewar, R Moseley, H Ostrer, et al.
Molecular Biology and Evolution
|
July 1, 1991
A Y-chromosomal DNA fragment is conserved in human and chimpanzee
B K Rasheed, E C Whisenant, R Fernandez, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 83) with videos related to
Sort By:
Page
of 9
Journal of Molecular Evolution
|
August 1, 1991
Evolution and sequence analysis of a human Y-chromosomal DNA fragment
E C Whisenant, B K Rasheed, H Ostrer, et al.
The Journal of Pediatrics
|
June 1, 1989
Familial XX chromosomal maleness does not arise from a Y chromosomal translocation
H Ostrer, G Wright, M Clayton, et al.
Clinical Dysmorphology
|
November 21, 1998
Acro-renal-ocular syndrome: expansion of the phenotype
E Guillén-Navarro, R Wallerstein, E Reich, et al.
American Journal of Human Genetics
|
December 1, 1988
Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes
E S Cantú, R D Marsh, K E Boecklen, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
January 7, 1998
X-inactivation and cytogenetic studies in a family with sensorineural hearing loss and Turner syndrome
N Sculerati, M A Perle, C Oddoux, et al.
British Journal of Haematology
|
December 24, 1997
Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11
B Wistinghausen, A Reischer, C Oddoux, et al.
Clinical Genetics
|
April 16, 2003
Genetic counseling for prostate cancer risk
A M Nieder, S S Taneja, M P A Zeegers, et al.
Experimental Cell Research
|
June 1, 1986
Human histone gene organization. Identification of a histone gene polymorphism prevalent in a black population
L Green, W Whittle, R Dell'Orco, et al.
JAMA
|
March 4, 1992
Genetic screening by insurance carriers
M A Dewar, R Moseley, H Ostrer, et al.
Molecular Biology and Evolution
|
July 1, 1991
A Y-chromosomal DNA fragment is conserved in human and chimpanzee
B K Rasheed, E C Whisenant, R Fernandez, et al.
Page
of 9