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Anomaly
Brevicollis
Congenital osseous torticollis syndrome
Congenital synostosis of the cervicothoraci vertebrae
Congenital webbed neck syndrome
Hereditary leukocytic hypersegmentation
Hyposegmentation
Klippel-Feil anomaly
Klippel-Feil disease
Klippel-Feil sign
Klippel-Feil syndrome
Leukomelanopathy
May-Hegglin
Pelger-Huët

Traduction de «anomaly syndrome alder » (Anglais → Français) :

Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy

Anomalie (granulation) (granulocyte) ou syndrome de:Alder | May-Hegglin | Pelger-Huët | Hypersegmentation | Hyposegmentation | leucocytaire, héréditaire | Leucomélanopathie héréditaire


A rare chromosomal anomaly syndrome characterized by pre and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, hand and foot anomalies (for example brachy/clinodactyly, talipes equinovarus, nail hypoplasi

monosomie distale 15q


A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are prenatal and postnatal growth delay, mild to severe intellectual disability, hemiatrophy, webbed neck, ocular and cutaneous pigmentary anomalies, cran

trisomie 22 en mosaïque


A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax

syndrome cranio-facio-fronto-digital


Klippel-Feil syndrome | Klippel-Feil anomaly | Klippel-Feil disease | Klippel-Feil sign | brevicollis | congenital osseous torticollis syndrome | congenital synostosis of the cervicothoraci vertebrae | congenital webbed neck syndrome

syndrome de Klippel-Feil | agénésie vertébrale cervicale | homme sans cou | syndrome de la réduction numérique cervicale




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Date index: 2022-01-15
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