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Following matter
Following text
Full position
IGF
International Graphical Federation
International Typographers' Secretariat
Nearest of blood
Nearest of kin
Next
Next Computer
Next Computer System
Next car
Next car indicator
Next lift
Next lift indicator
Next matter
Next of kin
Next of kin in blood
Next of kindred
Next to editorial matter
Next to reading matter
Next-of-kin
Next-to-reading matter
Typographers International

Translation of "next kindred " (English → French) :

nearest of blood | nearest of kin | next of kin | next of kindred | next-of-kin

plus proche parent | proches parents


nearest of blood [ nearest of kin | next of kindred | next of kin in blood | next-of-kin ]

plus proche parent


International Graphical Federation [ IGF | International Federation of Lithographers, Process Workers and Kindred Trades | International Federation of Bookbinders and Kindred Trades | International Typographers' Secretariat | Typographers International ]

Fédération graphique internationale [ FGI | International Federation of Lithographers, Process Workers and Kindred Trades | International Federation of Bookbinders and Kindred Trades | International Typographers' Secretariat | Internationale des typographes ]


Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s

ataxie spinocérébelleuse type 28


full position | next to reading matter | next-to-reading matter | next to editorial matter | following matter | following text | next matter

contre-texte | contre texte | à côté texte


Next Computer System [ Next | Next Computer ]

Next Computer System [ Next | ordinateur Next ]


next car | next lift

prochain ascenseur | prochain départ | prochaine cabine


next car indicator | next lift indicator

indicateur prochain ascenseur | indicateur prochain départ | indicateur prochaine cabine


Identified in Israeli Bedouin kindred the phenotype is similar to that of Lethal congenital contracture syndrome type 2 but without distended bladder. Affected individuals are born with severe multiple joint contractures with severe muscle wasting an

syndrome des contractures congénitales létales type 3


The combination of a propensity for venous thrombosis and seizures has been reported in two unrelated kindreds. Transmission is autosomal recessive. It results from a point mutation of PIGM, which reduces transcription of PIGM and blocks mannosylatio

syndrome d'hypercoagulabilité par déficit héréditaire en glycosyl phosphatidyl inositol




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Date index: 2021-11-02
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