#x-inactivation

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Neocentric X-chromosome in a girl with Turner-like syndrome
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Neocentric X-chromosome in a girl with Turner-like syndrome

Hemmat Morteza, Warburton, Yang Xiaojing, Boyar, El, Anguiano, Anguiano Arturo, Wang

Neocentric X-chromosome in a girl with Turner-like syndrome Alternate Text
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Savoirs

Neocentric X-chromosome in a girl with Turner-like syndrome

Hemmat Morteza, Warburton, Yang Xiaojing, Boyar, El, Anguiano, Anguiano Arturo, Wang

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6 pages

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Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy
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Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy

Juan-Mateu Jonàs, Nascimento Andrés, Jiménez-Mallebrera Cecilia, González-Quereda Lidia, Rivas Eloy, Paradas Carmen, Madruga Marcos, Sánchez-Ayaso Pedro, Jou Cristina, González-Mera Laura, Munell Francina, Roig-Quilis Manuel, Rabasa Maria, Hernández-Lain Aurelio, Díaz-Manera Jorge, Gallardo Eduard, Pascual Jordi, Verdura Edgard, Colomer Jaume, Baiget Montserrat, Olivé Montse, Gallano Pia, Rodriguez Maria

Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy Alternate Text
Category

Documents

Savoirs

Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy

Juan-Mateu Jonàs, Nascimento Andrés, Jiménez-Mallebrera Cecilia, González-Quereda Lidia, Rivas Eloy, Paradas Carmen, Madruga Marcos, Sánchez-Ayaso Pedro, Jou Cristina, González-Mera Laura, Munell Francina, Roig-Quilis Manuel, Rabasa Maria, Hernández-Lain Aurelio, Díaz-Manera Jorge, Gallardo Eduard, Pascual Jordi, Verdura Edgard, Colomer Jaume, Baiget Montserrat, Olivé Montse, Gallano Pia, Rodriguez Maria

Book

13 pages

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Preferential expression of mutant ABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms
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Preferential expression of mutant ABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms

Salsano Ettore, Tabano Silvia, Sirchia, Colapietro Patrizia, Castellotti Barbara, Gellera Cinzia, Rimoldi Marco, Pensato Viviana, Mariotti Caterina, Pareyson Davide, Miozzo Monica, Uziel Graziella

Preferential expression of mutant ABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms Alternate Text
Category

Documents

Savoirs

Preferential expression of mutant ABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms

Salsano Ettore, Tabano Silvia, Sirchia, Colapietro Patrizia, Castellotti Barbara, Gellera Cinzia, Rimoldi Marco, Pensato Viviana, Mariotti Caterina, Pareyson Davide, Miozzo Monica, Uziel Graziella

Book

9 pages

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English

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