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Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.

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Title: Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.
Authors: Kumar, Umesh1 (AUTHOR) umeshchandolia@rediffmail.com, Ray, Saugat2 (AUTHOR), Thapa, Amrit2 (AUTHOR), Walia, Baljinder Singh2 (AUTHOR), Chakrabarty, Barun Kumar3 (AUTHOR)
Source: Journal of Genetics. Jun2026, Vol. 105 Issue 1, p1-7. 7p.
Database: Academic Search Ultimate
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  Data: Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.
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  Data: <searchLink fieldCode="AR" term="%22Kumar%2C+Umesh%22">Kumar, Umesh</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> umeshchandolia@rediffmail.com</i><br /><searchLink fieldCode="AR" term="%22Ray%2C+Saugat%22">Ray, Saugat</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Thapa%2C+Amrit%22">Thapa, Amrit</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Walia%2C+Baljinder+Singh%22">Walia, Baljinder Singh</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chakrabarty%2C+Barun+Kumar%22">Chakrabarty, Barun Kumar</searchLink><relatesTo>3</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Genetics%22">Journal of Genetics</searchLink>. Jun2026, Vol. 105 Issue 1, p1-7. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=192831728
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        Value: 10.1007/s12041-026-01527-2
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      – Code: eng
        Text: English
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      – TitleFull: Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.
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            NameFull: Kumar, Umesh
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            NameFull: Ray, Saugat
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            NameFull: Thapa, Amrit
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              M: 06
              Text: Jun2026
              Type: published
              Y: 2026
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