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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/bf00394291.

Title:
The cri du chat syndrome | Human Genetics
Description:
Data for 331 cri du chat cases, including 34 Danish probands, are reviewed. The incidence and the prevalence among the mentally retarded population amounted to 1/45,000 and 1.5/1000, respectively. No striking association with prenatal events, parental ages, or birth order could be demonstrated. There was a significant excess of females. Parental translocations were present in slightly more than 10% of the families, while more rare cytogenetic aberrations (mosaicism, rings, and de novo translocations) accounted for less than 10% of all cases. The phenotypically relevant segment has been narrowed down to the midportion of the 5p15 band. Clinical, radiologic, and dermatoglyphic features are summarized and discussed, with special attention to the abnormal cry, which persists in many older probands, and to developmental abnormalities. No obvious correlation could be detected between clinical features and the localization of the deletion. No marker locus has yet been assigned to the short arm of chromosome 5. Treatment and prevention are briefly discussed.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Social Networks
  • Telecommunications

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

google, scholar, cri, chat, syndrome, chromosome, genet, med, criduchat, maladie, pediatr, ann, short, translocation, paris, case, cry, deletion, cat, lancet, humangenetik, arm, partial, niebuhr, dun, miller, del, hum, bras, dune, propos, cas, child, article, ment, délétion, paediatr, acta, human, cytogenetics, defic, lejeune, jpn, une, patients, clin, sindrome, clinical, cases, mentally,

Topics {✒️}

cri-du-chat-syndrom bei zwillingen une observation anatomo-clinique maladie du cri-du-chat ségrégation familiale d'une suspected cri-du-chat syndrome cri-du-chat syndrome combined propos d'une observation syndrome d'ehlers-danlos associ� cri-du-chat-syndrom cri-du-chat syndrome �cri-du-chat’ syndrome cri-du-chat syndrome apparent cri-du-chat month download article/chapter 32 cri-du-chat probands à propos d' cri-du-chat child une délétion autosomique le une nouvelle cri-du-chat cri du chat �cri du chat �cri-du-chat cri du chat �cri du chat �cri-du-chat la trisomie 5p marker locus étude d' une anomalie chromosomique york-san francisco-london das katzenschrei-syndrom liveborn birth-weight data b-group ring chromosome congenital heart disease red-cell triosephosphate isomerase découverte prénatale d' propos d' die chromosomalen syndrome de novo translocations multiple developmental anomalies de novo appearance deletion-translocation del privacy choices/manage cookies etude d' partial c-group trisomy chromosomal abnormality birth order de sa réciproque b-group chromosome

Questions {❓}

  • Mosaicism for a deleted chromosome 5?

Schema {🗺️}

WebPage:
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         headline:The cri du chat syndrome
         description:Data for 331 cri du chat cases, including 34 Danish probands, are reviewed. The incidence and the prevalence among the mentally retarded population amounted to 1/45,000 and 1.5/1000, respectively. No striking association with prenatal events, parental ages, or birth order could be demonstrated. There was a significant excess of females. Parental translocations were present in slightly more than 10% of the families, while more rare cytogenetic aberrations (mosaicism, rings, and de novo translocations) accounted for less than 10% of all cases. The phenotypically relevant segment has been narrowed down to the midportion of the 5p15 band. Clinical, radiologic, and dermatoglyphic features are summarized and discussed, with special attention to the abnormal cry, which persists in many older probands, and to developmental abnormalities. No obvious correlation could be detected between clinical features and the localization of the deletion. No marker locus has yet been assigned to the short arm of chromosome 5. Treatment and prevention are briefly discussed.
         datePublished:
         dateModified:
         pageStart:227
         pageEnd:275
         sameAs:https://doi.org/10.1007/BF00394291
         keywords:
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            Metabolic Disease
            Marker Locus
            Birth Order
            Developmental Abnormality
            Human Genetics
            Molecular Medicine
            Gene Function
            Metabolic Diseases
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ScholarlyArticle:
      headline:The cri du chat syndrome
      description:Data for 331 cri du chat cases, including 34 Danish probands, are reviewed. The incidence and the prevalence among the mentally retarded population amounted to 1/45,000 and 1.5/1000, respectively. No striking association with prenatal events, parental ages, or birth order could be demonstrated. There was a significant excess of females. Parental translocations were present in slightly more than 10% of the families, while more rare cytogenetic aberrations (mosaicism, rings, and de novo translocations) accounted for less than 10% of all cases. The phenotypically relevant segment has been narrowed down to the midportion of the 5p15 band. Clinical, radiologic, and dermatoglyphic features are summarized and discussed, with special attention to the abnormal cry, which persists in many older probands, and to developmental abnormalities. No obvious correlation could be detected between clinical features and the localization of the deletion. No marker locus has yet been assigned to the short arm of chromosome 5. Treatment and prevention are briefly discussed.
      datePublished:
      dateModified:
      pageStart:227
      pageEnd:275
      sameAs:https://doi.org/10.1007/BF00394291
      keywords:
         Internal Medicine
         Metabolic Disease
         Marker Locus
         Birth Order
         Developmental Abnormality
         Human Genetics
         Molecular Medicine
         Gene Function
         Metabolic Diseases
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                  name:The John F.Kennedy Institute
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                     name:The John F.Kennedy Institute, Glostrup, Denmark
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                  name:Children's Hospital at Vangede
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                     name:Children's Hospital at Vangede, Denmark
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         name:The John F.Kennedy Institute, Glostrup, Denmark
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               name:The John F.Kennedy Institute, Glostrup, Denmark
               type:PostalAddress
            type:Organization
            name:Children's Hospital at Vangede
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               name:Children's Hospital at Vangede, Denmark
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External Links {🔗}(258)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

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