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Nucléoprotéine C-terminale
Syndrome D
Syndrome de Bartholin-Patau
Syndrome de Patau
Syndrome de Smith-Patau
Trisomie 13-15
Trisomie 15 en mosaïque
Trisomie D1
Trisomie partielle du chromosome 13
Trisomie partielle du chromosome 15

Translation of "trisomie 13-15 " (French → English) :

trisomie 13-15
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
13-15D trisomy
médecine
médecine
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
syndrome de Bartholin-Patau | syndrome de Smith-Patau | syndrome de Patau | syndrome D | trisomie 13-15 | trisomie D1
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
Patau's syndrome | Bartholin-Patau syndrome | trisomy 13 syndrome | trisomy 13-15 syndrome | trisomy D syndrome | trisomy D1 syndrome
biologie > cytogénétique | biologie > embryologie | médecine > sémiologie et pathologie
biologie > cytogénétique | biologie > embryologie | médecine > sémiologie et pathologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
syndrome de Patau | trisomie 13-15
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
D1-trisomy syndrome
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
trisomie 15 en mosaïque
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
A rare chromosomal anomaly syndrome with principle characteristics of intrauterine growth restriction, congenital cardiac anomalies (ventricular and atrial septal defects, patent ductus arteriosus) and craniofacial dysmorphism (hypertelorism, downsla
SNOMEDCT-BE (disorder) / 764619001
SNOMEDCT-BE (ventricular and atrial septal defects, patent ductus arteriosus) and craniofacial dysmorphism (hypertelorism, downsla / 764619001
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
trisomie partielle du chromosome 15
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Duplication of chromosome 15
SNOMEDCT-BE (disorder) / 726354002
SNOMEDCT-BE (disorder) / 726354002
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
trisomie partielle du chromosome 13
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Duplication of chromosome 13
SNOMEDCT-BE (disorder) / 726352003
SNOMEDCT-BE (disorder) / 726352003
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Trisomie 13, translocation
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Trisomy 13, translocation
WORLD HEALTH ORGANIZATION ICD-10: Q91.6
WORLD HEALTH ORGANIZATION ICD-10: Q91.6
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Trisomie 13, mosaïque chromosomique (non-disjonction mitotique)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Trisomy 13, mosaicism (mitotic nondisjunction)
WORLD HEALTH ORGANIZATION ICD-10: Q91.5
WORLD HEALTH ORGANIZATION ICD-10: Q91.5
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Trisomie 13, non-disjonction méïotique
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Trisomy 13, meiotic nondisjunction
WORLD HEALTH ORGANIZATION ICD-10: Q91.4
WORLD HEALTH ORGANIZATION ICD-10: Q91.4
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
nucléoprotéine C-terminale | protéine 13/15 | p13/15 [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
protein 13/15 | p13/15 [Abbr.]
IATE - Health | Natural and applied sciences
IATE - Health | Natural and applied sciences
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]


Others have searched : trisomie 13 non-disjonction méïotique    trisomie 13 translocation    nucléoprotéine c-terminale    p13 15    protéine 13 15    syndrome    syndrome de bartholin-patau    syndrome de patau    syndrome de smith-patau    trisomie 13-15    trisomie 15 en mosaïque    trisomie d1    trisomie partielle du chromosome    


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trisomie 13-15

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