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F F Yen

Showing results (1-10 of 9) with videos related to

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Mechanisms of Ageing and Development|May 1, 1981
X chromatin and chromosome examination in aged womenF F Yen, S S Matsuyama, L F Jarvik
Clinical Genetics|August 18, 1999
Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocationL Amesse, F F Yen, B Weisskopf, et al.
American Journal of Medical Genetics|March 21, 1998
Changing phenotype in Floating-Harbor syndromeJ H Hersh, K R Groom, F F Yen, et al.
Fertility and Sterility|December 1, 1980
A case of familial XY gonadal dysgenesisJ H Hersh, W T Kable, F F Yen, et al.
Obstetrics and Gynecology|March 1, 1984
Gonadal and müllerian duct agenesis in a girl with 46,X,i(Xq)F D De Leon, J H Hersh, J S Sanfilippo, et al.
American Journal of Diseases of Children (1960)|January 1, 1985
Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution bandingJ H Hersh, K S Dale, P S Gerald, et al.
Clinical Genetics|March 31, 1998
Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormalityP G Williams, J H Hersh, F F Yen, et al.
Journal of Medical Genetics|April 1, 1995
De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: a clue to the locus of the candidate geneJ H Hersh, F F Yen, S C Peiper, et al.
American Journal of Medical Genetics|September 1, 1984
Tetraploidy: a report of three live-born infantsP R Scarbrough, J Hersh, M K Kukolich, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Mechanisms of Ageing and Development|May 1, 1981
X chromatin and chromosome examination in aged womenF F Yen, S S Matsuyama, L F Jarvik
Clinical Genetics|August 18, 1999
Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocationL Amesse, F F Yen, B Weisskopf, et al.
American Journal of Medical Genetics|March 21, 1998
Changing phenotype in Floating-Harbor syndromeJ H Hersh, K R Groom, F F Yen, et al.
Fertility and Sterility|December 1, 1980
A case of familial XY gonadal dysgenesisJ H Hersh, W T Kable, F F Yen, et al.
Obstetrics and Gynecology|March 1, 1984
Gonadal and müllerian duct agenesis in a girl with 46,X,i(Xq)F D De Leon, J H Hersh, J S Sanfilippo, et al.
American Journal of Diseases of Children (1960)|January 1, 1985
Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution bandingJ H Hersh, K S Dale, P S Gerald, et al.
Clinical Genetics|March 31, 1998
Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormalityP G Williams, J H Hersh, F F Yen, et al.
Journal of Medical Genetics|April 1, 1995
De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: a clue to the locus of the candidate geneJ H Hersh, F F Yen, S C Peiper, et al.
American Journal of Medical Genetics|September 1, 1984
Tetraploidy: a report of three live-born infantsP R Scarbrough, J Hersh, M K Kukolich, et al.
Pageof 1