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Experientia
|
November 15, 1975
Ring chromosomes and leukaemia
G 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 1q21
F Capon, S Semprini, B Dallapiccola, et al.
Journal of Medical Genetics
|
June 1, 1992
Acromegaloid facial appearance (AFA) syndrome: report of a second family
B 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 literature
B Dallapiccola, B Marino, A Giannotti, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1973
Skeletal changes in the "cri du chat" syndrome
B 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 reaction
G Novelli, M Gennarelli, M Rocchi, et al.
Human Genetics
|
December 15, 1976
Hand dermatoglyphics in trisomy 4p
P Mastroiacovo, V Currò, A Calabro, et al.
Chest
|
January 1, 1991
Di George anomaly with atrioventricular canal
B Marino, C Marcelletti, A Giannotti, et al.
American Journal of Medical Genetics
|
September 20, 2000
Familial mandibuloacral dysplasia: report of an additional Italian patient
C Tudisco, G Canepa, G Novelli, et al.
Clinical Chemistry
|
February 5, 2000
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma
P Amicucci, M Gennarelli, G Novelli, et al.
Page
of 48
Search research articles
Search
Showing results (101-110 of 479) with videos related to
Sort By:
Page
of 48
Experientia
|
November 15, 1975
Ring chromosomes and leukaemia
G 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 1q21
F Capon, S Semprini, B Dallapiccola, et al.
Journal of Medical Genetics
|
June 1, 1992
Acromegaloid facial appearance (AFA) syndrome: report of a second family
B 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 literature
B Dallapiccola, B Marino, A Giannotti, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1973
Skeletal changes in the "cri du chat" syndrome
B 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 reaction
G Novelli, M Gennarelli, M Rocchi, et al.
Human Genetics
|
December 15, 1976
Hand dermatoglyphics in trisomy 4p
P Mastroiacovo, V Currò, A Calabro, et al.
Chest
|
January 1, 1991
Di George anomaly with atrioventricular canal
B Marino, C Marcelletti, A Giannotti, et al.
American Journal of Medical Genetics
|
September 20, 2000
Familial mandibuloacral dysplasia: report of an additional Italian patient
C Tudisco, G Canepa, G Novelli, et al.
Clinical Chemistry
|
February 5, 2000
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma
P Amicucci, M Gennarelli, G Novelli, et al.
Page
of 48