Novel frameshift mutation of the NR0B1(DAX1) in two tall adult brothers

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1573-4978

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Novel frameshift mutation of the NR0B1(DAX1) in two tall adult brothers ; volume:46 ; number:4 ; day:6 ; month:7 ; year:2019 ; pages:4599-4604 ; date:8.2019
Molecular biology reports ; 46, Heft 4 (6.7.2019), 4599-4604, 8.2019

Creator: Bertalan, Rita
Bencsik, Zsuzsa
Mezei, Piroska
Vajda, Zsolt
Butz, Henriett
Patócs, Attila

Contributor: SpringerLink (Online service)

DOI: 10.1007/s11033-019-04688-9

URN: urn:nbn:de:101:1-2019122603545247362069

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:52 AM CEST

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Bertalan, Rita
Bencsik, Zsuzsa
Mezei, Piroska
Vajda, Zsolt
Butz, Henriett
Patócs, Attila
SpringerLink (Online service)

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Novel frameshift mutation of the NR0B1(DAX1) in two tall adult brothers

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Other Objects (12)

FMCGP: frameshift mutation cartesian genetic programming

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A new frameshift mutation of the β-spectrin gene associated with hereditary spherocytosis

A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle

A natural frameshift mutation in Campanula EIL2 correlates with ethylene insensitivity in flowers

Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12

Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation

Suppression einer mitochondrialen Frameshift-Mutation der Hefe Saccharomyces cerevisiae : bi-direktionale nukleo-mitochondriale Interaktion

Suppression einer mitochondrialen Frameshift-Mutation der Hefe Saccharomyces cerevisiae : bi-direktionale nukleo-mitochondriale Interaktion

Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature

A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle

FMCGP: frameshift mutation cartesian genetic programming

Muir-Torre-Syndrom mit bisher nicht beschriebener Frameshift-Mutation im MSH2-Gen

Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia

A new frameshift mutation of the β-spectrin gene associated with hereditary spherocytosis

A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle

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Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation

Suppression einer mitochondrialen Frameshift-Mutation der Hefe Saccharomyces cerevisiae : bi-direktionale nukleo-mitochondriale Interaktion

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FMCGP: frameshift mutation cartesian genetic programming

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Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia

A new frameshift mutation of the β-spectrin gene associated with hereditary spherocytosis

A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle

A natural frameshift mutation in Campanula EIL2 correlates with ethylene insensitivity in flowers

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Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation

Suppression einer mitochondrialen Frameshift-Mutation der Hefe Saccharomyces cerevisiae : bi-direktionale nukleo-mitochondriale Interaktion

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Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature

A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle

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