Class information for:
Level 1: CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
16716 575 20.0 65%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
409 16055 WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 CRI DU CHAT SYNDROME Author keyword 53 64% 9% 52
2 CRI DU CHAT Author keyword 27 92% 2% 11
3 3P DELETION SYNDROME Author keyword 17 100% 1% 8
4 TRISOMY 1Q Author keyword 15 63% 3% 15
5 PARTIAL TRISOMY 1Q Author keyword 13 69% 2% 11
6 3P SYNDROME Author keyword 12 86% 1% 6
7 5P DELETION SYNDROME Author keyword 11 100% 1% 6
8 TETRASOMY 5P Author keyword 11 100% 1% 6
9 DUP1Q Author keyword 8 100% 1% 5
10 CHROMOSOME 5 Author keyword 7 22% 5% 30

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 CRI DU CHAT SYNDROME 53 64% 9% 52 Search CRI+DU+CHAT+SYNDROME Search CRI+DU+CHAT+SYNDROME
2 CRI DU CHAT 27 92% 2% 11 Search CRI+DU+CHAT Search CRI+DU+CHAT
3 3P DELETION SYNDROME 17 100% 1% 8 Search 3P+DELETION+SYNDROME Search 3P+DELETION+SYNDROME
4 TRISOMY 1Q 15 63% 3% 15 Search TRISOMY+1Q Search TRISOMY+1Q
5 PARTIAL TRISOMY 1Q 13 69% 2% 11 Search PARTIAL+TRISOMY+1Q Search PARTIAL+TRISOMY+1Q
6 3P SYNDROME 12 86% 1% 6 Search 3P+SYNDROME Search 3P+SYNDROME
7 5P DELETION SYNDROME 11 100% 1% 6 Search 5P+DELETION+SYNDROME Search 5P+DELETION+SYNDROME
8 TETRASOMY 5P 11 100% 1% 6 Search TETRASOMY+5P Search TETRASOMY+5P
9 DUP1Q 8 100% 1% 5 Search DUP1Q Search DUP1Q
10 CHROMOSOME 5 7 22% 5% 30 Search CHROMOSOME+5 Search CHROMOSOME+5

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 3P SYNDROME 27 92% 2% 11
2 3P25 PTER 27 92% 2% 11
3 DUP3Q SYNDROME 21 64% 4% 21
4 CRI 14 51% 3% 20
5 DISTAL 5P 14 100% 1% 7
6 DISTAL 17Q 13 80% 1% 8
7 5P 13 41% 4% 24
8 1Q32 QTER 11 69% 2% 9
9 KARYOTYPE PHENOTYPE CORRELATION 11 78% 1% 7
10 CAT LIKE CRY 10 61% 2% 11

Journals

Reviews


Title Publ. year Cit. Active
references		 % act. ref.
to same field
Cri du chat syndrome 2006 36 66 82%
Cri du chat syndrome: A critical review 2010 6 10 100%
Mosaic tetrasomy 5p resulting from an isochromosome 5p marker chromosome: Case report and review of literature 2012 2 9 78%
Clinical, Cytogenetic and Molecular Study in a Case of r(3) with 3p Deletion and Review of the Literature 2011 3 24 67%
Speech and language development in cri du chat syndrome: A critical review 2008 8 27 48%
A terminal deletion of the short arm of chromosome 3: karyotype 46, XY, del (3) (p25-pter); a case report and literature review 2000 16 16 100%
Prenatal diagnosis of mosaic distal 5p deletion and review of the literature 2004 16 27 63%
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature 2012 1 15 60%
PARTIAL DUPLICATION 1Q - REPORT OF 4 PATIENTS AND REVIEW OF THE LITERATURE 1990 31 9 89%
A 649 kb microduplication in 1p34.1, including POMGNT1, in a patient with microcephaly, coloboma and laryngomalacia; and a review of the literature 2009 1 7 57%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ.
in class
1 N W BELFAST HLTH SOCIAL SERV TRUST 1 100% 0.3% 2
2 LINGUIST SCANDINAVIAN STUDIES 1 12% 1.2% 7
3 ABACID GENET 1 50% 0.2% 1
4 CLIN CHILD NEUROPSYCHOL 1 50% 0.2% 1
5 DEV NEUROPSYCHOL SERV 1 50% 0.2% 1
6 HISTOL CYTOL CYTOGENET 1 50% 0.2% 1
7 INFERTIL SEXOL 1 50% 0.2% 1
8 KINDER JUGENDMED KLIN 1 50% 0.2% 1
9 LEADERSHIP TEACHER EDUC 1 50% 0.2% 1
10 MED GENET DYSMORPHOL 1 50% 0.2% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000243391 TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P
2 0.0000185450 TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY
3 0.0000180668 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS
4 0.0000166868 JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER
5 0.0000163713 SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5
6 0.0000135581 PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//TRISOMY 12P
7 0.0000119527 RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15
8 0.0000115732 CAT EYE SYNDROME//SUPERNUMERARY MARKER CHROMOSOMES//SMALL SUPERNUMERARY MARKER CHROMOSOME
9 0.0000110539 CHROMOSOME 6Q DELETION//SIM1 GENE//6Q DELETION
10 0.0000108174 PITT HOPKINS SYNDROME//18Q DELETION SYNDROME//18Q SYNDROME