A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency.
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| Title: | A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency. |
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| Authors: | Parsons, Samuel J. H.1, Wright, Neville B.2, Burkitt‐Wright, Emma3,4, Skae, Mars S.5, Murray, Phillip G.1,5, philip.murray@manchester.ac.uk |
| Source: | American Journal of Medical Genetics. Part A; Aug2017, Vol. 173 Issue 8, p2261-2267, 7p |
| Database: | Applied Science & Technology Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: aci DbLabel: Applied Science & Technology Source An: 124091743 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Parsons%2C+Samuel+J%2E+H%2E%22">Parsons, Samuel J. H.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Wright%2C+Neville+B%2E%22">Wright, Neville B.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AU" term="%22Burkitt‐Wright%2C+Emma%22">Burkitt‐Wright, Emma</searchLink><relatesTo>3,4</relatesTo><br /><searchLink fieldCode="AU" term="%22Skae%2C+Mars+S%2E%22">Skae, Mars S.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AU" term="%22Murray%2C+Phillip+G%2E%22">Murray, Phillip G.</searchLink><relatesTo>1,5</relatesTo>, <i>philip.murray@manchester.ac.uk</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22American+Journal+of+Medical+Genetics%2E+Part+A%22">American Journal of Medical Genetics. Part A</searchLink>; Aug2017, Vol. 173 Issue 8, p2261-2267, 7p |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=124091743 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.38306 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 2261 Titles: – TitleFull: A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Parsons, Samuel J. H. – PersonEntity: Name: NameFull: Wright, Neville B. – PersonEntity: Name: NameFull: Burkitt‐Wright, Emma – PersonEntity: Name: NameFull: Skae, Mars S. – PersonEntity: Name: NameFull: Murray, Phillip G. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2017 Type: published Y: 2017 Identifiers: – Type: issn-print Value: 15524825 Numbering: – Type: volume Value: 173 – Type: issue Value: 8 Titles: – TitleFull: American Journal of Medical Genetics. Part A Type: main |
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