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B Dallapiccola

Showing results (101-110 of 479) with videos related to

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Experientia|November 15, 1975
Ring chromosomes and leukaemiaG Alimena, L Annino, B Dallapiccola, et al.
American Journal of Human Genetics|December 1, 1999
Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21F Capon, S Semprini, B Dallapiccola, et al.
Journal of Medical Genetics|June 1, 1992
Acromegaloid facial appearance (AFA) syndrome: report of a second familyB Dallapiccola, L Zelante, L Accadia, et al.
Annales De Genetique|January 1, 1989
Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literatureB Dallapiccola, B Marino, A Giannotti, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1973
Skeletal changes in the "cri du chat" syndromeB Dallapiccola, G Pistocchi, A Forabosco, et al.
Human Genetics|March 1, 1992
Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reactionG Novelli, M Gennarelli, M Rocchi, et al.
Human Genetics|December 15, 1976
Hand dermatoglyphics in trisomy 4pP Mastroiacovo, V Currò, A Calabro, et al.
Chest|January 1, 1991
Di George anomaly with atrioventricular canalB Marino, C Marcelletti, A Giannotti, et al.
American Journal of Medical Genetics|September 20, 2000
Familial mandibuloacral dysplasia: report of an additional Italian patientC Tudisco, G Canepa, G Novelli, et al.
Clinical Chemistry|February 5, 2000
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasmaP Amicucci, M Gennarelli, G Novelli, et al.
Pageof 48

Showing results (101-110 of 479) with videos related to

Sort By:
Pageof 48
Experientia|November 15, 1975
Ring chromosomes and leukaemiaG Alimena, L Annino, B Dallapiccola, et al.
American Journal of Human Genetics|December 1, 1999
Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21F Capon, S Semprini, B Dallapiccola, et al.
Journal of Medical Genetics|June 1, 1992
Acromegaloid facial appearance (AFA) syndrome: report of a second familyB Dallapiccola, L Zelante, L Accadia, et al.
Annales De Genetique|January 1, 1989
Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literatureB Dallapiccola, B Marino, A Giannotti, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1973
Skeletal changes in the "cri du chat" syndromeB Dallapiccola, G Pistocchi, A Forabosco, et al.
Human Genetics|March 1, 1992
Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reactionG Novelli, M Gennarelli, M Rocchi, et al.
Human Genetics|December 15, 1976
Hand dermatoglyphics in trisomy 4pP Mastroiacovo, V Currò, A Calabro, et al.
Chest|January 1, 1991
Di George anomaly with atrioventricular canalB Marino, C Marcelletti, A Giannotti, et al.
American Journal of Medical Genetics|September 20, 2000
Familial mandibuloacral dysplasia: report of an additional Italian patientC Tudisco, G Canepa, G Novelli, et al.
Clinical Chemistry|February 5, 2000
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasmaP Amicucci, M Gennarelli, G Novelli, et al.
Pageof 48