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Syndrome de chromosome 9 en anneau
Syndrome du chromosome 12 en anneau
Syndrome du chromosome 16 en anneau
Syndrome du chromosome 17 en anneau
Syndrome du chromosome 2 en anneau
Syndrome du chromosome 3 en anneau
Syndrome du chromosome 5 en anneau
Syndrome du chromosome 6 en anneau
Syndrome du chromosome 7 en anneau
Syndrome du chromosome Y en anneau

Translation of "Syndrome du chromosome 5 en anneau " (French → English) :

syndrome du chromosome 5 en anneau

A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are a neonatal mewing cry, severe developmental delay and intellectual disability, short stature, hypotonia, dysmorphic features (including microcephaly,
SNOMEDCT-BE (disorder) / 765487008
SNOMEDCT-BE (including microcephaly, / 765487008


syndrome du chromosome 2 en anneau

A rare chromosomal anomaly syndrome with highly variable phenotype. Principal characteristics are intrauterine growth retardation, failure to thrive, developmental delay, hypotonia, mild dysmorphic features (including microcephaly, short forehead, up
SNOMEDCT-BE (disorder) / 765485000
SNOMEDCT-BE (including microcephaly, short forehead, up / 765485000


syndrome du chromosome 7 en anneau

A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are growth failure, short stature, intellectual disability, dermatological abnormalities (nevus flammeus, dark pigmented nevi, cafe au lait spots), microc
SNOMEDCT-BE (disorder) / 765489006
SNOMEDCT-BE (nevus flammeus, dark pigmented nevi, cafe au lait spots), microc / 765489006


syndrome du chromosome Y en anneau

A rare chromosome Y structural anomaly, with a highly variable phenotype, mostly characterised by short stature, partial to total gonadal failure, sexual infantilism, genital anomalies (e.g. ambiguous genitalia, hypospadias, cryptorchidism), and azoo
SNOMEDCT-BE (disorder) / 763407008
SNOMEDCT-BE (e.g. ambiguous genitalia, hypospadias, cryptorchidism), and azoo / 763407008


syndrome du chromosome 6 en anneau

Ring chromosome 6 syndrome
SNOMEDCT-BE (disorder) / 765488003
SNOMEDCT-BE (disorder) / 765488003


syndrome du chromosome 3 en anneau

Ring chromosome 3
SNOMEDCT-BE (disorder) / 765486004
SNOMEDCT-BE (disorder) / 765486004


syndrome du chromosome 16 en anneau

Ring chromosome 16
SNOMEDCT-BE (disorder) / 763406004
SNOMEDCT-BE (disorder) / 763406004


syndrome du chromosome 12 en anneau

Ring chromosome 12
SNOMEDCT-BE (disorder) / 770595006
SNOMEDCT-BE (disorder) / 770595006


syndrome du chromosome 17 en anneau

Ring 17
SNOMEDCT-BE (disorder) / 778043005
SNOMEDCT-BE (disorder) / 778043005


syndrome de chromosome 9 en anneau

Ring chromosome 9 syndrome
SNOMEDCT-BE (disorder) / 60650002
SNOMEDCT-BE (disorder) / 60650002




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Syndrome du chromosome 5 en anneau

Date index:2022-04-16 -

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