facial dysmorphism
Filipino_translation
dysmorphism present
Filipino_translation
body dysmorphism
Filipino_translation
dysmorphism observed
Filipino_translation
dysmorphism absent
Filipino_translation
no dysmorphism
Filipino_translation
the patient exhibited signs of facial dysmorphism.
Naitala ng geneticista ang facial dysmorphism sa unang pagsusuri.
doctors identified subtle skeletal dysmorphism during the examination.
Maaaring hindi mapansin ang banayad na craniofacial dysmorphism kung walang maingat na pisikal na pagsusuri.
genetic testing confirmed a syndrome characterized by digital dysmorphism.
Napansin sa ulat ang dysmorphism na naaayon sa isang kilalang sindroma.
body dysmorphism often requires specialized cognitive behavioral therapy.
Naobserbahan ng pediatrician ang dysmorphism at nirekomenda ang bata para sa genetic testing.
severe craniofacial dysmorphism was observed in the newborn.
Sinuri ang mga clinical photos upang masuri ang dysmorphism sa paglipas ng panahon.
the study focused on the detection of mild dysmorphism.
Sinamahan ng banayad na dysmorphism ang developmental delay sa ilang mga kaso.
characteristic dysmorphism includes widely spaced eyes and low-set ears.
Tinalakay ng team ang dysmorphism bilang bahagi ng differential diagnosis.
body dysmorphism disorder is a chronic mental health condition.
Inilarawan nila ang dysmorphism na nakakaapekto sa mga tainga at nasal bridge.
the diagnosis relies on recognizing patterns of congenital dysmorphism.
Gumamit ang clinician ng standardized terms upang ilarawan ang dysmorphism.
researchers analyzed images to quantify the degree of dysmorphism.
Hindi halata ang dysmorphism, ngunit nakakabahala pa rin ang family history.
prenatal ultrasound screening can sometimes detect physical dysmorphism.
Inutos ang karagdagang imaging dahil pinaghihinalaan ang skeletal dysmorphism.
facial dysmorphism
Filipino_translation
dysmorphism present
Filipino_translation
body dysmorphism
Filipino_translation
dysmorphism observed
Filipino_translation
dysmorphism absent
Filipino_translation
no dysmorphism
Filipino_translation
the patient exhibited signs of facial dysmorphism.
Naitala ng geneticista ang facial dysmorphism sa unang pagsusuri.
doctors identified subtle skeletal dysmorphism during the examination.
Maaaring hindi mapansin ang banayad na craniofacial dysmorphism kung walang maingat na pisikal na pagsusuri.
genetic testing confirmed a syndrome characterized by digital dysmorphism.
Napansin sa ulat ang dysmorphism na naaayon sa isang kilalang sindroma.
body dysmorphism often requires specialized cognitive behavioral therapy.
Naobserbahan ng pediatrician ang dysmorphism at nirekomenda ang bata para sa genetic testing.
severe craniofacial dysmorphism was observed in the newborn.
Sinuri ang mga clinical photos upang masuri ang dysmorphism sa paglipas ng panahon.
the study focused on the detection of mild dysmorphism.
Sinamahan ng banayad na dysmorphism ang developmental delay sa ilang mga kaso.
characteristic dysmorphism includes widely spaced eyes and low-set ears.
Tinalakay ng team ang dysmorphism bilang bahagi ng differential diagnosis.
body dysmorphism disorder is a chronic mental health condition.
Inilarawan nila ang dysmorphism na nakakaapekto sa mga tainga at nasal bridge.
the diagnosis relies on recognizing patterns of congenital dysmorphism.
Gumamit ang clinician ng standardized terms upang ilarawan ang dysmorphism.
researchers analyzed images to quantify the degree of dysmorphism.
Hindi halata ang dysmorphism, ngunit nakakabahala pa rin ang family history.
prenatal ultrasound screening can sometimes detect physical dysmorphism.
Inutos ang karagdagang imaging dahil pinaghihinalaan ang skeletal dysmorphism.
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