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No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B.

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Title: No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B.
Authors: Ibrahim, Iman1 (AUTHOR), Scriver, Tara2 (AUTHOR), Basalom, Shuaa A.2 (AUTHOR) shuaa.basalom@saskhealthauthority.ca
Source: Clinical Case Reports. May2023, Vol. 11 Issue 5, p1-7. 7p.
Database: Academic Search Ultimate
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  Data: No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B.
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  Data: <searchLink fieldCode="AR" term="%22Ibrahim%2C+Iman%22">Ibrahim, Iman</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Scriver%2C+Tara%22">Scriver, Tara</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Basalom%2C+Shuaa+A%2E%22">Basalom, Shuaa A.</searchLink><relatesTo>2</relatesTo> (AUTHOR)<i> shuaa.basalom@saskhealthauthority.ca</i>
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  Data: <searchLink fieldCode="JN" term="%22Clinical+Case+Reports%22">Clinical Case Reports</searchLink>. May2023, Vol. 11 Issue 5, p1-7. 7p.
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        Value: 10.1002/ccr3.7332
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      – Code: eng
        Text: English
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        PageCount: 7
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      – TitleFull: No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B.
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            NameFull: Ibrahim, Iman
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            NameFull: Scriver, Tara
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            NameFull: Basalom, Shuaa A.
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            – D: 01
              M: 05
              Text: May2023
              Type: published
              Y: 2023
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              Value: 11
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              Value: 5
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            – TitleFull: Clinical Case Reports
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