11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1752-1947

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report ; volume:12 ; number:1 ; day:8 ; month:1 ; year:2018 ; pages:1-4 ; date:12.2018
Journal of medical case reports ; 12, Heft 1 (8.1.2018), 1-4, 12.2018

Keyword: Erbkrankheit
Erbschaden

Creator: Ichimiya, Yuko

Contributor: Wada, Yuka
Kunishima, Shinji
Tsukamoto, Keiko
Kosaki, Rika
Sago, Haruhiko
Ishiguro, Akira
Ito, Yushi
SpringerLink (Online service)

DOI: 10.1186/s13256-017-1535-5

URN: urn:nbn:de:1111-2018030210000

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:00 AM CEST

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Ichimiya, Yuko
Wada, Yuka
Kunishima, Shinji
Tsukamoto, Keiko
Kosaki, Rika
Sago, Haruhiko
Ishiguro, Akira
Ito, Yushi
SpringerLink (Online service)

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Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

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Jacobsen syndrome: Chromosome deletion at llq23

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Partial deletion of distal long arm encompassing Jacobsen Syndrome

Jacobsen syndrome and neonatal bleeding: report on two unrelated patients

Deletion 22q13.3 syndrome

Severe anal bleeding in Proteus syndrome: a case report

Complement Activation in 22q11.2 Deletion Syndrome

Familial deletion 18p syndrome: case report

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption?

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

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Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

Jacobsen syndrome: Chromosome deletion at llq23

Jacobsen syndrome

Partial deletion of distal long arm encompassing Jacobsen Syndrome

Jacobsen syndrome and neonatal bleeding: report on two unrelated patients

Deletion 22q13.3 syndrome

Severe anal bleeding in Proteus syndrome: a case report

Complement Activation in 22q11.2 Deletion Syndrome

Familial deletion 18p syndrome: case report

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption?

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

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Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

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11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report

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Other Objects (12)

Jacobsen syndrome: Chromosome deletion at llq23

Jacobsen syndrome

Partial deletion of distal long arm encompassing Jacobsen Syndrome

Jacobsen syndrome and neonatal bleeding: report on two unrelated patients

Deletion 22q13.3 syndrome

Severe anal bleeding in Proteus syndrome: a case report

Complement Activation in 22q11.2 Deletion Syndrome

Familial deletion 18p syndrome: case report

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption?

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

Jacobsen syndrome: Chromosome deletion at llq23

Jacobsen syndrome

Partial deletion of distal long arm encompassing Jacobsen Syndrome

Jacobsen syndrome and neonatal bleeding: report on two unrelated patients

Deletion 22q13.3 syndrome

Severe anal bleeding in Proteus syndrome: a case report

Complement Activation in 22q11.2 Deletion Syndrome

Familial deletion 18p syndrome: case report

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption?

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

Jacobsen syndrome: Chromosome deletion at llq23

Jacobsen syndrome

Partial deletion of distal long arm encompassing Jacobsen Syndrome

Jacobsen syndrome and neonatal bleeding: report on two unrelated patients

Deletion 22q13.3 syndrome

Severe anal bleeding in Proteus syndrome: a case report

Complement Activation in 22q11.2 Deletion Syndrome

Familial deletion 18p syndrome: case report

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption?

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

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