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A Rosenmann

Showing results (21-30 of 29) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|April 1, 1980
Amniotic fluid 3,3',5'-triiodothyronine in the detection of congenital hypothyroidismH Landau, J Sack, H Frucht, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 12, 1999
Prenatal diagnosis of oculocutaneous albinism type I: review and personal experienceE Rosenmann, A Rosenmann, Z Ne'eman, et al.
Cytogenetics and Cell Genetics|January 1, 1978
A long unidentifiable extra chromosomal segment--a possible duplication of human 7qJ Wahrman, M M Cohen, A Rosenmann, et al.
American Journal of Human Genetics|April 1, 1994
Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in IsraelR Gershoni-Baruch, A Rosenmann, S Droetto, et al.
Prenatal Diagnosis|April 1, 1995
DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A)T C Falik-Borenstein, S A Holmes, Z Borochowitz, et al.
The American Journal of Medicine|October 1, 1975
Chromatin-positive Klinefelter's syndrome with undetectable peripheral FSH levelsD Rabinowitz, M M Cohen, E Rosenmann, et al.
Urology|August 1, 1986
Persistent müllerian structures in infertile maleA Hershlag, I M Spitz, D Hochner-Celnikier, et al.
Human Molecular Genetics|May 1, 1997
Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingN C Arbour, J Zlotogora, R G Knowlton, et al.
Human Mutation|January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)R A Spritz, S T Lee, K Fukai, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1980
Amniotic fluid 3,3',5'-triiodothyronine in the detection of congenital hypothyroidismH Landau, J Sack, H Frucht, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 12, 1999
Prenatal diagnosis of oculocutaneous albinism type I: review and personal experienceE Rosenmann, A Rosenmann, Z Ne'eman, et al.
Cytogenetics and Cell Genetics|January 1, 1978
A long unidentifiable extra chromosomal segment--a possible duplication of human 7qJ Wahrman, M M Cohen, A Rosenmann, et al.
American Journal of Human Genetics|April 1, 1994
Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in IsraelR Gershoni-Baruch, A Rosenmann, S Droetto, et al.
Prenatal Diagnosis|April 1, 1995
DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A)T C Falik-Borenstein, S A Holmes, Z Borochowitz, et al.
The American Journal of Medicine|October 1, 1975
Chromatin-positive Klinefelter's syndrome with undetectable peripheral FSH levelsD Rabinowitz, M M Cohen, E Rosenmann, et al.
Urology|August 1, 1986
Persistent müllerian structures in infertile maleA Hershlag, I M Spitz, D Hochner-Celnikier, et al.
Human Molecular Genetics|May 1, 1997
Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingN C Arbour, J Zlotogora, R G Knowlton, et al.
Human Mutation|January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)R A Spritz, S T Lee, K Fukai, et al.
Pageof 3