Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183). (Q36689665)

15 August 2017

Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183). (English)

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M P Mulder

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M Wilke

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A Langeveld

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A Hagemeijer

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E van Drunen

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E C Zwarthoff

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P H Riegman

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W H Deelen

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A M van den Ouweland

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1 August 1995

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https://scigraph.springernature.com/pub.10.1007/bf00207368

15 August 2017

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DiGeorge syndrome and 22q11 rearrangements

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DiGeorge anomaly associated with 10p deletion

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A new polymorphic probe on chromosome 22: NB84 (D22S183)

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Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

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Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

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The spectrum of the DiGeorge syndrome

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Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

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Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

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Cytogenetic findings in a prospective series of patients with DiGeorge anomaly

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The DiGeorge anomaly as a developmental field defect

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Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).

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12 December 2020

In situ hybridization and translocation breakpoint mapping. III. DiGeorge syndrome with partial monosomy of chromosome 22

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12 December 2020

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome

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12 December 2020

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization

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Identifiers

DOI

10.1007/BF00207368

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15 August 2017

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