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A Notarangelo

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

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Prenatal Diagnosis|November 1, 1994
The 18ph+ chromosome heteromorphismL Zelante, A Notarangelo, B Dallapiccola
Human Genetics|July 1, 1986
Ring chromosome 21 in healthy persons: different consequences in females and in malesB Dallapiccola, V De Filippis, A Notarangelo, et al.
Annales De Genetique|June 24, 2003
Interstitial "de novo" tandem duplication of 7(q31.1-q35): first reported caseL Zelante, A I Croce, A Grifa, et al.
Annales De Genetique|January 1, 1994
Cytogenetic and molecular analysis of trisomy 9. Case report and reviewL Zelante, A Notarangelo, A I Croce, et al.
Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.
Annales De Genetique|October 17, 2002
A complex mosaicism 45,X/46,X,del(Xq)/46,X,idic(Xq) in a patient with secondary amenorrheaS Calvano, G P de Cillis, A I Croce, et al.
American Journal of Human Genetics|October 1, 1995
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneityP Gasparini, M J Calonge, L Bisceglia, et al.
Genomics|August 29, 1998
Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletionsM Centra, E Memeo, M d'Apolito, et al.
Molecular and Cellular Probes|August 1, 1993
The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphismsE Trabetti, R Galavotti, L Zanini, et al.
American Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.
Pageof 1

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

Sort By:
Pageof 1
Prenatal Diagnosis|November 1, 1994
The 18ph+ chromosome heteromorphismL Zelante, A Notarangelo, B Dallapiccola
Human Genetics|July 1, 1986
Ring chromosome 21 in healthy persons: different consequences in females and in malesB Dallapiccola, V De Filippis, A Notarangelo, et al.
Annales De Genetique|June 24, 2003
Interstitial "de novo" tandem duplication of 7(q31.1-q35): first reported caseL Zelante, A I Croce, A Grifa, et al.
Annales De Genetique|January 1, 1994
Cytogenetic and molecular analysis of trisomy 9. Case report and reviewL Zelante, A Notarangelo, A I Croce, et al.
Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.
Annales De Genetique|October 17, 2002
A complex mosaicism 45,X/46,X,del(Xq)/46,X,idic(Xq) in a patient with secondary amenorrheaS Calvano, G P de Cillis, A I Croce, et al.
American Journal of Human Genetics|October 1, 1995
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneityP Gasparini, M J Calonge, L Bisceglia, et al.
Genomics|August 29, 1998
Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletionsM Centra, E Memeo, M d'Apolito, et al.
Molecular and Cellular Probes|August 1, 1993
The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphismsE Trabetti, R Galavotti, L Zanini, et al.
American Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.
Pageof 1