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A Ilicki

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Human Genetics|February 1, 1997
Genetic and linkage analysis of familial congenital hypothyroidism: exclusion of linkage to the TSH receptor geneB D Ahlbom, M Yaqoob, A Larsson, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Linkage analysis excludes familial congenital hypothyroidism from chromosome 21B E Ahlbom, M Yaqoob, G Annerén, et al.
Acta Paediatrica Scandinavica|November 1, 1984
Premature thelarche--natural history and sex hormone secretion in 68 girlsA Ilicki, R Prager Lewin, R Kauli, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Gene conversion in the CYP11B2 gene encoding P450c11AS is associated with, but does not cause, the syndrome of corticosterone methyloxidase II deficiencyC E Fardella, D W Hum, H Rodriguez, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Human Genetics|February 1, 1997
Genetic and linkage analysis of familial congenital hypothyroidism: exclusion of linkage to the TSH receptor geneB D Ahlbom, M Yaqoob, A Larsson, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Linkage analysis excludes familial congenital hypothyroidism from chromosome 21B E Ahlbom, M Yaqoob, G Annerén, et al.
Acta Paediatrica Scandinavica|November 1, 1984
Premature thelarche--natural history and sex hormone secretion in 68 girlsA Ilicki, R Prager Lewin, R Kauli, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Gene conversion in the CYP11B2 gene encoding P450c11AS is associated with, but does not cause, the syndrome of corticosterone methyloxidase II deficiencyC E Fardella, D W Hum, H Rodriguez, et al.
Pageof 2