Exact(55)
It is supposed to be a prank, a great, vulgar cri de coeur revealing a truth hitherto hidden away: parents resent their kids for depriving them of sleep.
He calls for the gradual creation of a "system of checks and balances".This is the muffled cri de coeur of a reasonable and decent man who, still only 52, now feels obliged to work for the World Bank in Washington, DC.
If so, his heroic cri de coeur is less a rallying cry for a beleaguered industry than a harbinger of further decline and decay.
Because the government does not want to raise taxes to fund these plans, public spending is forecast to fall from 41% of GDP today to just 35% by the end of the decade.That has prompted accusations that the government wants the country to go back to the late-1930s and late-1930s andwell describes in his cri de coeur againstheoverty.
In his 1989 book "Transplant" (part memoir, part cri de coeur about organ transplants) he was resolutely scientific rather than theological on the question of when life begins and ends.
His essay made it clear that he believes the recent rejection of the constitution was a cri de coeur from Europe's voters to protect their precious subsidies from more competition, inside or outside the EU.
Similar(5)
In humans, cri-du-chat syndrome is caused by a heterozygous deletion at the tip of the short arm of chromosome 5. Infants are born with this condition as the result of a deletion arising in parental germinal tissues or even in sex cells.
The minority of cri-du-chat cases are inherited; the parent who carries the genetic abnormality typically is unaffected by the disorder, owing to a phenomenon known as balanced translocation (chromosomal rearrangement in which there is no net gain or loss of genetic material).
Cri-du-chat syndrome, also called 5p− syndrome, cat cry syndrome, or Lejeune syndrome, congenital disorder caused by partial deletion of the short arm of chromosome 5.
See also Down syndrome; cri-du-chat syndrome; trisomy 13; trisomy 18; Turner's syndrome; X-trisomy; Klinefelter's syndrome; XYY-trisomy.
Cri-du-chat syndrome is diagnosed in infants and young children on the basis of clinical symptoms and may be confirmed through chromosomal analysis.
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