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Search Results - Rosser, Lyndon G.
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Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene
by
Ørstavik, Karen Helene
,
Knudsen, Gun Peggy S.
,
Nordgarden, Hilde
,
Ormerod, Eli
,
Strømme, Petter
,
Lazarou, Lazarous P.
,
Rosser, Lyndon G.
,
Prescott, Trine
,
Houge, Gunnar
Published in
American journal of medical genetics. Part A
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Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene
by
Rosser, Lyndon G.
,
McKee, Shane
,
Millar, David S.
,
Archer, Hayley
,
Hughes, James
,
Butler, Rachel
,
Chuzhanova, Nadia
,
Cooper, David N.
,
Lazarou, Lazarus P.
Published in
Genomic medicine
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Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene
by
Ørstavik, Karen Helene
,
Knudsen, Gun Peggy S.
,
Nordgarden, Hilde
,
Ormerod, Eli
,
Strømme, Petter
,
Lazarou, Lazarous P.
,
Rosser, Lyndon G.
,
Prescott, Trine
,
Houge, Gunnar
Published in
American Journal of Medical Genetics Part A
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American Journal Of Medical Genetics. Part A
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Genomic Medicine
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The Hugo Journal
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Hypohidrotic Ectodermal Dysplasia
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X Chromosome Inactivation
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Biological And Medical Sciences
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Biomedical And Life Sciences
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Biomedicine
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Child, Preschool
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Chromosome Painting
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Chromosomes, Human, Pair 9 - Genetics
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Chromosomes, Human, X - Genetics
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Dermatology
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Ectodermal Dysplasia - Diagnosis
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Ectodermal Dysplasia - Genetics
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Ectodysplasins - Genetics
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Facial Bones, Jaws, Teeth, Parodontium: Diseases, Semeiology
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Familial Non-Identical Mutations
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Female
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Genetic Linkage
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Genetics & Heredity
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Hair - Abnormalities
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Hair And Nails Disorders
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