(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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15 August 2017

4

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15 August 2017

M P Mulder

1

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15 August 2017

M Wilke

2

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15 August 2017

A Langeveld

3

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15 August 2017

A Hagemeijer

5

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15 August 2017

E van Drunen

6

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15 August 2017

E C Zwarthoff

7

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15 August 2017

P H Riegman

8

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15 August 2017

W H Deelen

9

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15 August 2017

A M van den Ouweland

10

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15 August 2017

1 August 1995

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15 August 2017

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15 August 2017

96

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15 August 2017

133-141

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15 August 2017

2

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

15 August 2017

0 references

cites work

A prospective cytogenetic study of 36 cases of DiGeorge syndrome

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12 December 2020

Velo-cardio-facial syndrome: a review of 120 patients.

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12 December 2020

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

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12 December 2020

DiGeorge syndrome and 22q11 rearrangements

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12 December 2020

Deletions within chromosome 22q11 in familial congenital heart disease

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12 December 2020

DiGeorge anomaly associated with 10p deletion

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12 December 2020

Isolation and characterization of 25 unique DNA markers for human chromosome 22.

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12 December 2020

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

1 reference

12 December 2020

Male-to-male transmission of the velo-cardio-facial syndrome: a case report and review of 60 cases

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12 December 2020

Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.

1 reference

12 December 2020

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

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12 December 2020

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.

1 reference

12 December 2020

Toward a long-range map of human chromosomal band 22q11.

1 reference

12 December 2020

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

1 reference

12 December 2020

DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin

1 reference

12 December 2020

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

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12 December 2020

Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei

1 reference

12 December 2020

Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.

1 reference

12 December 2020

Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.

1 reference

12 December 2020

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 reference

12 December 2020

The spectrum of the DiGeorge syndrome

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12 December 2020

Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Detection of the Philadelphia chromosome in interphase nuclei

1 reference

12 December 2020

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

1 reference

12 December 2020

Dependence of thymus development on derivatives of the neural crest

1 reference

12 December 2020

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

1 reference

12 December 2020

The velo-cardio-facial syndrome: a clinical and genetic analysis

1 reference

12 December 2020

Cytogenetic findings in a prospective series of patients with DiGeorge anomaly

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12 December 2020

The DiGeorge anomaly as a developmental field defect

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

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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12 December 2020

Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases

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12 December 2020

DiGeorge syndrome: part of CATCH 22.

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12 December 2020

Di George anomaly and velocardiofacial syndrome.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00207368

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15 August 2017

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