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Niels Tommerup
Niels Tommerup
Genetics
Chromosomal translocation
Biology
Phenotype
Breakpoint
5
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61
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0.02
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Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes
2018
Tiia Maria Luukkonen
Mana M. Mehrjouy
Minna Pöyhönen
Anna-Kaisa Anttonen
Päivi Lahermo
Pekka Ellonen
Lars Paulin
Niels Tommerup
Aarno Palotie
Teppo Varilo
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Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes
2018
Tiia Maria Luukkonen
Mana M. Mehrjouy
Minna Pöyhönen
Anna-Kaisa Anttonen
Päivi Lahermo
Pekka Ellonen
Lars Paulin
Niels Tommerup
Aarno Palotie
Teppo Varilo
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Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes
2018
Tiia Maria Luukkonen
Mana M. Mehrjouy
Minna Pöyhönen
Anna-Kaisa Anttonen
Päivi Lahermo
Pekka Ellonen
Lars Paulin
Niels Tommerup
Aarno Palotie
Teppo Varilo
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Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes
2018
Tiia Maria Luukkonen
Mana M. Mehrjouy
Minna Pöyhönen
Anna-Kaisa Anttonen
Päivi Lahermo
Pekka Ellonen
Lars Paulin
Niels Tommerup
Aarno Palotie
Teppo Varilo
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A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly‐craniofacial anomalies syndrome
1983
American Journal of Medical Genetics
Niels Tommerup
Finn Cilius Nielsen
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Citations (61)
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