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M Fraccaro

Showing results (61-70 of 64) with videos related to

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Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Human Genetics|January 1, 1981
Sex-reversed XY females with campomelic dysplasia are H-Y negativeF D Bricarelli, M Fraccaro, J Lindsten, et al.
Human Molecular Genetics|December 1, 1996
Homozygous and compound heterozygous mutations at the Werner syndrome locusJ Oshima, C E Yu, C Piussan, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
Pageof 7

Showing results (61-70 of 64) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 64 results.
Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Human Genetics|January 1, 1981
Sex-reversed XY females with campomelic dysplasia are H-Y negativeF D Bricarelli, M Fraccaro, J Lindsten, et al.
Human Molecular Genetics|December 1, 1996
Homozygous and compound heterozygous mutations at the Werner syndrome locusJ Oshima, C E Yu, C Piussan, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
Pageof 7