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E Sarret

Showing results (1-10 of 19) with videos related to

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Helvetica Paediatrica Acta|June 1, 1971
Triploid live full-term infantJ Prats, E Sarret, A Moragas, et al.
Acta Obstetrica Y Ginecologica Hispano-Lusitana|March 1, 1979
[Pure gonadal dysgenesis and Klinefelter's syndrome in a sterile couple]R Blanco, C Foradada, M Usandizaga-Calparsoro, et al.
Revista Clinica Espanola|June 15, 1979
[Chronic myeloid leukemia (Ph1 positive) in Turner's syndrome (45, XO)]A Julia, C Sánchez, J M Tresanchez, et al.
Jornal De Pediatria|November 1, 1995
[Beals-Hecht Syndrome: report of a neonatal case]V A Ramos, C A Sastre, E Sarret, et al.
Prenatal Diagnosis|May 1, 1994
Terminal deletion of Xp in a dysmorphic anencephalic fetusA Plaja, T Vendrell, E Sarret, et al.
Annales De Genetique|December 8, 2004
Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bendingA Plaja, R Miro, E Lloveras, et al.
American Journal of Medical Genetics|June 8, 2001
Bends in human mitotic metaphase chromosomes revisited: 15q11-13 is the most frequent non-random autosomal bend in blood culturesA Plaja, R Miró, C Fuster, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Prenatal diagnosis of a rare chromosomal instability syndrome: variegated aneuploidy related to premature centromere division (PCD)A Plaja, C Mediano, L Cano, et al.
Annales De Genetique|May 26, 1998
Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetusA Plaja, C Mediano, I Farran, et al.
Medicina Clinica|September 1, 1982
[Pregnancy in a woman having Turner syndrome with 45,X/46,XX/47,XXX mosaicism]X Formiguera Sala, A M Sanmartí Sala, E Sarret Grau, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Helvetica Paediatrica Acta|June 1, 1971
Triploid live full-term infantJ Prats, E Sarret, A Moragas, et al.
Acta Obstetrica Y Ginecologica Hispano-Lusitana|March 1, 1979
[Pure gonadal dysgenesis and Klinefelter's syndrome in a sterile couple]R Blanco, C Foradada, M Usandizaga-Calparsoro, et al.
Revista Clinica Espanola|June 15, 1979
[Chronic myeloid leukemia (Ph1 positive) in Turner's syndrome (45, XO)]A Julia, C Sánchez, J M Tresanchez, et al.
Jornal De Pediatria|November 1, 1995
[Beals-Hecht Syndrome: report of a neonatal case]V A Ramos, C A Sastre, E Sarret, et al.
Prenatal Diagnosis|May 1, 1994
Terminal deletion of Xp in a dysmorphic anencephalic fetusA Plaja, T Vendrell, E Sarret, et al.
Annales De Genetique|December 8, 2004
Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bendingA Plaja, R Miro, E Lloveras, et al.
American Journal of Medical Genetics|June 8, 2001
Bends in human mitotic metaphase chromosomes revisited: 15q11-13 is the most frequent non-random autosomal bend in blood culturesA Plaja, R Miró, C Fuster, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Prenatal diagnosis of a rare chromosomal instability syndrome: variegated aneuploidy related to premature centromere division (PCD)A Plaja, C Mediano, L Cano, et al.
Annales De Genetique|May 26, 1998
Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetusA Plaja, C Mediano, I Farran, et al.
Medicina Clinica|September 1, 1982
[Pregnancy in a woman having Turner syndrome with 45,X/46,XX/47,XXX mosaicism]X Formiguera Sala, A M Sanmartí Sala, E Sarret Grau, et al.
Pageof 2