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O T Mueller

Showing results (21-30 of 25) with videos related to

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American Journal of Human Genetics|October 11, 1991
Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpointO T Mueller, J K Hartsfield, L A Gallardo, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1992
Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasiaS Pang, A T Clark, L C Freeman, et al.
American Journal of Medical Genetics|July 31, 2001
Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XXM J Sutcliffe, O T Mueller, B G Kousseff, et al.
American Journal of Human Genetics|April 1, 1990
The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivationP L Chang, O T Mueller, R M Lafrenie, et al.
Molecular Endocrinology (Baltimore, Md.)|March 1, 1991
A homozygous deletion in the c-erbA beta thyroid hormone receptor gene in a patient with generalized thyroid hormone resistance: isolation and characterization of the mutant receptorS J Usala, J B Menke, T L Watson, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
American Journal of Human Genetics|October 11, 1991
Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpointO T Mueller, J K Hartsfield, L A Gallardo, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1992
Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasiaS Pang, A T Clark, L C Freeman, et al.
American Journal of Medical Genetics|July 31, 2001
Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XXM J Sutcliffe, O T Mueller, B G Kousseff, et al.
American Journal of Human Genetics|April 1, 1990
The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivationP L Chang, O T Mueller, R M Lafrenie, et al.
Molecular Endocrinology (Baltimore, Md.)|March 1, 1991
A homozygous deletion in the c-erbA beta thyroid hormone receptor gene in a patient with generalized thyroid hormone resistance: isolation and characterization of the mutant receptorS J Usala, J B Menke, T L Watson, et al.
Pageof 3