Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients (Q35881635)

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16 October 2019

title

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients (English)

1 reference

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16 October 2019

main subject

Smith-Magenis syndrome

1 reference

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16 October 2019

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16 October 2019

R C Juyal

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16 October 2019

X Hauge

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16 October 2019

S H Elsea

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16 October 2019

J R Lupski

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16 October 2019

F Greenberg

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16 October 2019

A Baldini

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16 October 2019

language of work or name

English

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publication date

1 May 1996

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American Journal of Human Genetics

16 October 2019

published in

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16 October 2019

volume

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16 October 2019

issue

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16 October 2019

page(s)

998-1007

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Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome

16 October 2019

cites work

1 reference

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Mosaicism for deletion 17p11.2 in a boy with the Smith-Magenis syndrome

11 July 2018

1 reference

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High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridization

11 July 2018

1 reference

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Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis

11 July 2018

1 reference

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A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels

11 July 2018

1 reference

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The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2

11 July 2018

1 reference

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The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients

11 July 2018

1 reference

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Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

11 July 2018

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The 1993-94 Généthon human genetic linkage map

11 July 2018

1 reference

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Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.

11 July 2018

1 reference

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Interstitial deletion of 17p11.2: case report and review

11 July 2018

1 reference

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Chromosome subband 17p11.2 deletion: a minute deletion syndrome.

11 July 2018

1 reference

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Genetic analysis of NF1: identification of close flanking markers on chromosome 17.

11 July 2018

1 reference

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Genes for human U3 small nucleolar RNA contain highly conserved flanking sequences

11 July 2018

1 reference

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Interstitial deletion of (17)(p11.2p11.2) in nine patients

11 July 2018

1 reference

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Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements

11 July 2018

1 reference

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Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p11.2 p11.2) (Smith-Magenis syndrome).

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

Three polymorphisms at the D17S29 locus.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases

11 July 2018

1 reference

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Diagnostic hand anomalies in Smith-Magenis syndrome: Four new patients with del (17)(p11.2p11.2)

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

Two MspI RFLPs at the D17S258 locus

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

On the parental origin of de novo mutation in man.

11 July 2018

1 reference

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Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p

11 July 2018

1 reference

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Characterization of a low copy repetitive element S232 involved in the generation of frequent deletions of the distal short arm of the human X chromosome

11 July 2018

1 reference

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The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

11 July 2018

1 reference

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Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome

11 July 2018

1 reference

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Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

27 July 2018

1 reference

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Clinical and chromosome studies of three patients with Smith-Magenis syndrome

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914618

Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region

24 September 2018

1 reference

12 December 2020

Multiple variants in subtelomeric regions of normal karyotypes

1 reference

12 December 2020

Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome

1 reference

12 December 2020

Eye abnormalities in the Smith-Magenis contiguous gene deletion syndrome

1 reference

12 December 2020

Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A

1 reference

12 December 2020

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion

1 reference

12 December 2020

Prenatal diagnosis of interstitial deletion of 17(p11.2p11.2) (Smith-Magenis syndrome)

1 reference

12 December 2020

The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome

1 reference

12 December 2020

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17

1 reference

12 December 2020

Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters

1 reference

12 December 2020

Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization

1 reference

12 December 2020

Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient

1 reference

12 December 2020

Interstitial deletion of the short arm of chromosome 17

1 reference

12 December 2020

Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17

1 reference

12 December 2020

Identifiers

1 reference

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16 October 2019

PubMed publication ID

8651284

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