ChromosomendeletionMeSH Deskriptor

https://www.has-sante.fr/jcms/p_3390484/fr/deletion-10q26
2022
false
false
false
chromosomen, menschliche, paar 10
chromosomendeletion
facies
lernstörungen
genetische beratung
differentialdiagnose
patientenschulung
schwangerschaft
chronische krankheit

---
https://www.has-sante.fr/jcms/p_3291595/fr/syndrome-de-kleefstra
2021
false
false
false
fallmanagement
herzfehler, kongenitale
chromosomen, menschliche, paar 9
geistige retardierung
chromosomendeletion
kraniofaziale fehlbildungen
geistige retardierung

---
https://www.has-sante.fr/jcms/p_3097438/fr/microdeletion-2q37
2019
false
true
false
false
Mikrodeletionssyndrom 2q37
chromosomen, menschliche, paar 2
chromosomendeletion
fallmanagement

---
https://www.orpha.net/data/patho/Han/Int/fr/PhelanMcDermid_FR_fr_HAN_ORPHA48652.pdf
2019
false
true
false
false
chromosomen, menschliche, paar 22
chromosomendeletion
chromosomenstörungen
chromosomenstörungen
chromosomenstörungen
chromosomenstörungen
chromosomenstörungen

---
https://www.rarechromo.org/media/translations/Francais/3p25%20Deletions%20French%20QFN.pdf
2014
chromosomendeletion
chromosomen, menschliche, paar 3

---
https://www.rarechromo.org/media/translations/Francais/6q%20Deletions%206q%20de%206q26%20a%206q27%20Francais%20FTNW.pdf
https://www.rarechromo.org/media/translations/Francais/6q%20Deletions%206q%20de%206q26%20a%206q27%20Francais%20FTNP.pdf
2014
false
false
false
chromosomendeletion
chromosomen, menschliche, paar 6
Chromosom 6-Deletion, partielle
kind, neugeborenes
kleinkind
kind

---
https://www.rarechromo.org/media/translations/Francais/13q%20Deletions%20de%20la%20region%2013q%20terminale%20French%20FTNW.pdf
2013
false
true
false
chromosomen, menschliche, paar 13
chromosomenaberrationen
kindesentwicklung
chromosomendeletion
chromosomenstörungen

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=1620
chromosomendeletion
chromosomen, menschliche, paar 3
seltene krankheiten

---
https://www.rarechromo.org/media/translations/Francais/10q26%20Deletions%20French%20QFN.pdf
2012
false
true
false
chromosomen, menschliche, paar 10
chromosomendeletion
kindesentwicklung
lernstörungen
facies

---
http://www.smithmagenis.com/
abnormitäten, multiple
chromosomendeletion
geistige retardierung

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=251056
2011
false
true
false
chromosomendeletion
kleinkind
Mikrodeletionssyndrom 6q25
entwicklungsbedingte fähigkeitsstörungen
kraniofaziale fehlbildungen
schwerhörigkeit, schallempfindungs-
kind
chromosomen, menschliche, paar 6

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=251014
2011
false
true
false
kleinkind
Mikrodeletionssyndrom 2q31.1
chromosomen, menschliche, paar 2
entwicklungsbedingte fähigkeitsstörungen
abnormitäten, multiple
kraniofaziale fehlbildungen
wachstumsstörungen
chromosomendeletion
kind

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=251019
2011
false
true
false
kleinkind
chromosomendeletion
geistige retardierung
abnormitäten, multiple
Mikrodeletionssyndrom 2q32q33
chromosomen, menschliche, paar 2
kind

---
https://www.rarechromo.org/media/translations/Francais/17q21.31%20Microdeletions%20French%20FTNW.pdf
2010
chromosomendeletion
chromosomen, menschliche, paar 17
Koolen-de Vries-Syndrom

---
https://www.rarechromo.org/media/translations/Francais/2q32%20Deletions%20et%20MicroDeletions%20French%20FTNW.pdf
2010
false
false
chromosomendeletion
chromosomenstörungen

---
https://www.rarechromo.org/media/translations/Francais/5q22%20Deletions%20incluant%20la%20region%205q22%20French%20QFN.pdf
2010
chromosomendeletion
chromosomenstörungen
chromosomen, menschliche, paar 5

---
https://www.rarechromo.org/media/translations/Francais/22q13%20Deletions%20Syndrome%20de%20Phelan%20McDermid%20French%20QFN.pdf
2009
chromosomen, menschliche, paar 22
chromosomendeletion
chromosomenstörungen

---
https://www.rarechromo.org/media/translations/Francais/1p36%20Syndrome%20de%20la%20Deletion%201p36%20French%20QFN.pdf
2009
chromosomen, menschliche, paar 1
chromosomendeletion
chromosomenstörungen

---
https://www.rarechromo.org/media/translations/Francais/2q37%20Deletions%20French%20QFN.pdf
2009
chromosomendeletion
chromosomen, menschliche, paar 2

---
https://www.jle.com/fr/revues/medecine/hma/e-docs/00/04/3D/75/resume.md
2008
chromosomendeletion
histon-acetyltransferasen
leukämie, myeloische, akute

---
https://www.jle.com/fr/revues/medecine/hma/e-docs/00/04/40/F5/resume.md
2008
chromosomen, menschliche, paar 5
myelodysplastische syndrome
chromosomendeletion
myelodysplastische syndrome
thalidomid
antitumormittel
myelodysplastische syndrome

---
https://www.rarechromo.org/media/translations/Francais/9p%20Deletions%20French%20QFN.pdf
2007
chromosomendeletion
chromosomen, menschliche, paar 9

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=1646
2006
seltene krankheiten
chromosomendeletion
geschlechtschromosomale aberrationen
chromosomen, menschliche, y
chromosomale störungen der geschlechtsentwicklung

---
http://atlasgeneticsoncology.org/Educ/MicrodeletionID30059FS.html
2006
chromosomendeletion
molekularbiologie
di-george-syndrom
prader-willi-syndrom
angelman-syndrom
neurofibromatose 1
gene, neurofibromatose-1-
williams-syndrom
phänotyp
chromosomen, menschliche, paar 17
chromosomen, menschliche, paar 8

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=1597
2006
chromosomendeletion
chromosomen, menschliche, paar 17

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=75857
2006
chromosomendeletion
abnormitäten, multiple

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=52022
2006
chromosomendeletion
seltene krankheiten
chromosomen, menschliche, paar 11
chromosomenstörungen

---
http://www.has-sante.fr/portail/display.jsp?id=c_500291
http://www.has-sante.fr/portail/display.jsp?id=c_500274
2006
true
y-chromosom
infertilität, männliche
chromosomendeletion
infertilität, männliche

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=1617
2004
seltene krankheiten
chromosomen, menschliche, paar 2
chromosomendeletion

---