A common region of 10p deleted in DiGeorge and velocardiofacial syndromes (Q57251931)

10

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Thomas Meitinger

object named as

Thomas Meitinger

7

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Judith A Goodship

9

object named as

Judith Goodship

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author name string

Sara C.M. Daw

1

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Catherine Taylor

2

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Kathy Call

4

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Jen-i Mao

5

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Simone Schuffenhauer

6

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Tony Lipson

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

8

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publication date

August 1996

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language of work or name

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13

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issue

4

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page(s)

458-460

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cites work

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DiGeorge syndrome: part of CATCH 22.

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Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

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An STS-based map of the human genome

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

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7 January 2021

Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

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Assignment of the gene encoding the beta-subunit of the human fibronectin receptor (beta-FNR) to chromosome 10p11.2

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Fine genetic mapping of the proximal part of mouse chromosome 2 excludes Pax-8 as a candidate gene for Danforth's short tail (Sd)

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Yeast artificial chromosome libraries containing large inserts from mouse and human DNA

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Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism

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Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome

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An optimized Alu-PCR primer pair for human-specific amplification of YACs and somatic cell hybrids

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A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

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High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

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7 January 2021