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Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features
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| Zeitschriftentitel: | Human Mutation |
|---|---|
| Personen und Körperschaften: | , , , , , , , , , , , , , , |
| In: | Human Mutation, 41, 2020, 7, S. 1238-1249 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Hindawi Limited
|
| Schlagwörter: |
| author_facet |
Ballout, Rami A. Dickerson, Cheryl Wick, Myra J. Al‐Sweel, Najla Openshaw, Amanda S. Srivastava, Siddharth Swanson, Lindsay C. Bramswig, Nuria C. Kuechler, Alma Hong, Bo Fleming, Leah R. Curry, Kathryn Robertson, Stephen P. Andersen, Erica F. El‐Hattab, Ayman W. Ballout, Rami A. Dickerson, Cheryl Wick, Myra J. Al‐Sweel, Najla Openshaw, Amanda S. Srivastava, Siddharth Swanson, Lindsay C. Bramswig, Nuria C. Kuechler, Alma Hong, Bo Fleming, Leah R. Curry, Kathryn Robertson, Stephen P. Andersen, Erica F. El‐Hattab, Ayman W. |
|---|---|
| author |
Ballout, Rami A. Dickerson, Cheryl Wick, Myra J. Al‐Sweel, Najla Openshaw, Amanda S. Srivastava, Siddharth Swanson, Lindsay C. Bramswig, Nuria C. Kuechler, Alma Hong, Bo Fleming, Leah R. Curry, Kathryn Robertson, Stephen P. Andersen, Erica F. El‐Hattab, Ayman W. |
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Ballout, Rami A. Dickerson, Cheryl Wick, Myra J. Al‐Sweel, Najla Openshaw, Amanda S. Srivastava, Siddharth Swanson, Lindsay C. Bramswig, Nuria C. Kuechler, Alma Hong, Bo Fleming, Leah R. Curry, Kathryn Robertson, Stephen P. Andersen, Erica F. El‐Hattab, Ayman W. Human Mutation Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features Genetics (clinical) Genetics |
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Ballout, Rami A. Dickerson, Cheryl Wick, Myra J. Al‐Sweel, Najla Openshaw, Amanda S. Srivastava, Siddharth Swanson, Lindsay C. Bramswig, Nuria C. Kuechler, Alma Hong, Bo Fleming, Leah R. Curry, Kathryn Robertson, Stephen P. Andersen, Erica F. El‐Hattab, Ayman W. 1059-7794 1098-1004 Hindawi Limited Genetics (clinical) Genetics http://dx.doi.org/10.1002/humu.24009 <i>Int22h1/Int22h2</i> ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features Human Mutation |
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| title |
Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_unstemmed |
Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_full |
Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_fullStr |
Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_full_unstemmed |
Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_short |
Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_sort |
<i>int22h1/int22h2</i>
‐mediated xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| topic |
Genetics (clinical) Genetics |
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http://dx.doi.org/10.1002/humu.24009 |
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2020 |
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| spelling | Ballout, Rami A. Dickerson, Cheryl Wick, Myra J. Al‐Sweel, Najla Openshaw, Amanda S. Srivastava, Siddharth Swanson, Lindsay C. Bramswig, Nuria C. Kuechler, Alma Hong, Bo Fleming, Leah R. Curry, Kathryn Robertson, Stephen P. Andersen, Erica F. El‐Hattab, Ayman W. 1059-7794 1098-1004 Hindawi Limited Genetics (clinical) Genetics http://dx.doi.org/10.1002/humu.24009 <i>Int22h1/Int22h2</i> ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features Human Mutation |
| spellingShingle | Ballout, Rami A., Dickerson, Cheryl, Wick, Myra J., Al‐Sweel, Najla, Openshaw, Amanda S., Srivastava, Siddharth, Swanson, Lindsay C., Bramswig, Nuria C., Kuechler, Alma, Hong, Bo, Fleming, Leah R., Curry, Kathryn, Robertson, Stephen P., Andersen, Erica F., El‐Hattab, Ayman W., Human Mutation, Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features, Genetics (clinical), Genetics |
| title | Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_full | Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_fullStr | Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_full_unstemmed | Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_short | Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_sort | <i>int22h1/int22h2</i> ‐mediated xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| title_unstemmed | Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features |
| topic | Genetics (clinical), Genetics |
| url | http://dx.doi.org/10.1002/humu.24009 |