₁Catherine Fallet-Bianco

Summary for 2002 [at-glance overview of Catherine Fallet-Bianco work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Catherine Fallet-Bianco. According to available data, in 2002 Catherine Fallet-Bianco published at least 1 articles. This work was completed in collaboration with several authors including Encha-Razavi, Ferechte and Delezoide, Anne-Lise. There is no information about the funding or the grants awarded to support this work.

Analysis of the article abstracts and the titles suggests that Catherine Fallet-Bianco professional interests are focused around "unusual variant holoprosencephaly", "holoprosencephaly monosomy 13q" and "variant holoprosencephaly monosomy". These might also be referred to as "monosomy 13q", "arm chromosome" or "variant holoprosencephaly". Statistical analysis shows that Catherine Fallet-Bianco's writing is likely to contains terms "holoprosencephaly", "13q", "cases", "unusual", "leads" and "variant".

The majority of Catherine Fallet-Bianco articles are affiliated with Service d'Anatomie Pathologique, CHU, Hôpital Morvan, 29609 Brest Cedex, France. Sadly, no email addresses were found for any of the affiliations.

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Alternative names (1) [other authors with names similar to Catherine Fallet-Bianco]

₁₈Fallet-Bianco, C

Year 2002 Charts [Catherine Fallet-Bianco frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Catherine Fallet-Bianco publication and funding history for the range of years]

Catherine Fallet-Bianco Coauthors (5) [all coauthors with the number of joint publications]

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1

₅Encha-Razavi, Ferechte

1

₄Delezoide, Anne-Lise

1

₁Loget, Philippe

1

₁Marcorelles, Pascale

1

₁Roume, Joëlle

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Affiliations (1) [condensed summary of the Catherine Fallet-Bianco affiliations, the leading number and the color conveys importance]

₁Service d'Anatomie Pathologique, CHU, Hôpital Morvan, 29609 Brest Cedex, France.

Key Opinion Leader In [Catherine Fallet-Bianco is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

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Keywords (11) [keywords assigned to Catherine Fallet-Bianco articles by PubMed, the leading number and the color conveys importance]

₁Pregnancy | ₁Cerebral Cortex | ₁Holoprosencephaly | ₁Adult | ₁Transcription Factors | ₁Humans | ₁Chromosome Deletion | ₁Female | ₁Chromosomes, Human, Pair 13 | ₁Syndrome | ₁Male

Catherine Fallet-Bianco Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Catherine Fallet-Bianco might be a good expert witness on these terms]

₅holoprosencephaly | ₄13q | ₂cases | ₂unusual | ₂leads | ₂variant | ₂monosomy | ₂arm | ₂related | ₂type | ₂chromosome | ₂particular | ₂gene | ₂zic2 | ₁described | ₁deletion | ₁human | ₁anomaly | ₁stages | ₁malformations | ₁midline | ₁gestation | ₁cerebral | ₁may | ₁clover-shaped | ₁clinical | ₁various | ₁syntelencephaly | ₁especially | ₁findings | ₁so-called | ₁includes
₂monosomy 13q | ₂arm chromosome | ₂variant holoprosencephaly | ₂unusual variant | ₂type holoprosencephaly | ₂holoprosencephaly monosomy | ₁may related | ₁particular type | ₁13q fetuses | ₁trimesters gestation | ₁findings suggest | ₁chromosome so-called | ₁loss function | ₁interhemispheric fusion | ₁magnetic resonance | ₁q32 unusual | ₁cerebral midline | ₁imaging eight | ₁anomaly leads | ₁cases cerebral | ₁report describes | ₁zic2 gene | ₁related zic2 | ₁includes considerable | ₁clinical phenotype | ₁phenotype related | ₁gestation malformation | ₁cases compared | ₁human gene | ₁13q cases | ₁recently human | ₁midline anomaly
₂unusual variant holoprosencephaly | ₂holoprosencephaly monosomy 13q | ₂variant holoprosencephaly monosomy | ₁middle interhemispheric fusion | ₁so-called 13q syndrome | ₁tomography magnetic resonance | ₁findings suggest | ₁reviews recently human | ₁malformations especially brain | ₁related zic2 gene | ₁monosomy 13q cases | ₁terminal deletion arm | ₁syndrome includes considerable | ₁malformation described computer | ₁mutation leads holoprosencephaly | ₁different stages third | ₁stages third trimesters | ₁report describes | ₁third trimesters gestation | ₁ages called middle | ₁interhemispheric fusion syntelencephaly | ₁resonance imaging eight | ₁eight children various | ₁loss function unusual | ₁trimesters gestation malformation | ₁report describes cases | ₁gene zic2 mutation | ₁deletion arm chromosome | ₁type holoprosencephaly may | ₁cases compared literature | ₁may related zic2 | ₁findings

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