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S P Dahoun

Showing results (1-10 of 7) with videos related to

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Annales De Genetique|October 20, 1999
Pure partial trisomy 5q33-->5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocationA Paoloni-Giacobino, A Bottani, S P Dahoun
Annales De Genetique|November 6, 2001
A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISHA Paoloni-Giacobino, J Lespinasse, I Moix, et al.
Clinical Genetics|June 11, 1999
A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysisA Paoloni-Giacobino, M H Dutoit, M A Morris, et al.
Human Genetics|May 14, 1999
Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic levelJ C Barber, C J Reed, S P Dahoun, et al.
Archives of General Psychiatry|February 7, 2001
Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary studyS Eliez, S E Antonarakis, M A Morris, et al.
Clinical Genetics|November 15, 2000
Familial t(6;21)(p21.1;p13) translocation associated with male-only sterilityA Paoloni-Giacobino, I Kern, Y Rumpler, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|June 3, 2000
A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonographyA Paoloni-Giacobino, S P Dahoun, P C Sizonenko, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Annales De Genetique|October 20, 1999
Pure partial trisomy 5q33-->5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocationA Paoloni-Giacobino, A Bottani, S P Dahoun
Annales De Genetique|November 6, 2001
A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISHA Paoloni-Giacobino, J Lespinasse, I Moix, et al.
Clinical Genetics|June 11, 1999
A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysisA Paoloni-Giacobino, M H Dutoit, M A Morris, et al.
Human Genetics|May 14, 1999
Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic levelJ C Barber, C J Reed, S P Dahoun, et al.
Archives of General Psychiatry|February 7, 2001
Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary studyS Eliez, S E Antonarakis, M A Morris, et al.
Clinical Genetics|November 15, 2000
Familial t(6;21)(p21.1;p13) translocation associated with male-only sterilityA Paoloni-Giacobino, I Kern, Y Rumpler, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|June 3, 2000
A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonographyA Paoloni-Giacobino, S P Dahoun, P C Sizonenko, et al.
Pageof 1