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Results of search for 'su:"Cri-du-Chat Syndrome"', page 25 of 34
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Authors
Atkins, L
Berger, R
Breg, W R
Chen, Chih-Ping
Chern, Schu-Rern
Dallapiccola, B
Danesino, Cesare
Engel, E
Fryns, J P
Guala, Andrea
Kristoffersen, Kristian Emil
Lafourcade, J
Lejeune, J
Marinescu, R C
Niebuhr, E
Oliver, Chris
Overhauser, J
Pastore, G
Spunton, Marianna
Wasmuth, J J
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Topics
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 5
Cri-du-Chat Syndrome
Female
Humans
Infant
Infant, Newborn
Karyotyping
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Trisomy
complications
diagnosis
genetics
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481.
Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat).
[electronic resource]
by
Levy, Brynn
Dunn, Teresa M
Kern, Jeffrey H
Hirschhorn, Kurt
Kardon, Nataline B
Producer:
20020403
In:
American journal of medical genetics
vol. 108
Online resources:
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482.
The dual face of endogenous alpha-aminoketones: pro-oxidizing metabolic weapons.
[electronic resource]
by
Bechara, Etelvino J H
Dutra, Fernando
Cardoso, Vanessa E S
Sartori, Adriano
Olympio, Kelly P K
Penatti, Carlos A A
Adhikari, Avishek
Assunção, Nilson A
Producer:
20071002
In:
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP
vol. 146
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483.
Cri du Chat syndrome: Characteristics of 73 Brazilian patients.
[electronic resource]
by
Honjo, R S
Mello, C B
Pimenta, L S E
Nuñes-Vaca, E C
Benedetto, L M
Khoury, R B F
Befi-Lopes, D M
Kim, C A
Producer:
20191114
In:
Journal of intellectual disability research : JIDR
vol. 62
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484.
Anesthetic considerations in cri du chat syndrome: a report of three cases.
[electronic resource]
by
Yamashita, M
Tanioka, F
Taniguchi, K
Matsuki, A
Oyama, T
Producer:
19850827
In:
Anesthesiology
vol. 63
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485.
[Indications for chromosome analysis in childhood].
[electronic resource]
by
Goetz, P
Kucerová, M
Macek, M
Producer:
19700701
In:
Ceskoslovenska pediatrie
vol. 25
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486.
A de novo cryptic 5p deletion and 9p duplication detected by subtelomeric MLPA in a boy with cri du chat syndrome.
[electronic resource]
by
Lincoln-de-Carvalho, Carolina R
Vicente, Fabíola M P
Vieira, Társis A P
de Mello, Maricilda P
Marques-de-Faria, Antonia P
Producer:
20110520
In:
American journal of medical genetics. Part A
vol. 155A
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487.
Feasibility and Reliability of Functional Mobility Measures in Children With Cri du Chat (5P-) Syndrome.
[electronic resource]
by
Abbruzzese, Laurel D
Ruggeri, Anneliese R
Esquerre, Jennifer C
Patel, Prina
Raske, Lisa
Producer:
20201102
In:
Pediatric physical therapy : the official publication of the Section on Pediatrics of the American Physical Therapy Association
vol. 32
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488.
Measurements on hand radiographs from 32 cri-du-chat probands.
[electronic resource]
by
Fenger, K
Niebuhr, E
Producer:
19781129
In:
Radiology
vol. 129
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489.
Translocation 4p-- syndrome: a general review.
[electronic resource]
by
Centerwall, W R
Thompson, W P
Allen, I E
Fobes, C D
Producer:
19750626
In:
American journal of diseases of children (1960)
vol. 129
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490.
Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
[electronic resource]
by
Sreekantaiah, C
Kronn, D
Marinescu, R C
Goldin, B
Overhauser, J
Producer:
19991105
In:
American journal of medical genetics
vol. 86
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491.
Microarray delineation of familial chromosomal imbalance with deletion 5q35 and duplication 10q25 in a child showing multiple anomalies and dysmorphism.
[electronic resource]
by
Masri, Amira
Gimelli, Stefania
Hamamy, Hanan
Sloan-Béna, Frédérique
Producer:
20150819
In:
American journal of medical genetics. Part A
vol. 164A
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492.
Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma.
[electronic resource]
by
Zhao, Chen
Tynan, John
Ehrich, Mathias
Hannum, Gregory
McCullough, Ron
Saldivar, Juan-Sebastian
Oeth, Paul
van den Boom, Dirk
Deciu, Cosmin
Producer:
20150526
In:
Clinical chemistry
vol. 61
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493.
Ocular findings in a patient with deletion short arm chromosome 5 (cri du chat) and ring chromosome 14.
[electronic resource]
by
Clark, D I
Howard, P J
Patterson, A
Producer:
19871110
In:
Transactions of the ophthalmological societies of the United Kingdom
vol. 105 ( Pt 6)
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494.
[Chromosome disease. I. Autosomal syndromes].
[electronic resource]
by
Malygina, N A
Producer:
19851220
In:
Fel'dsher i akusherka
vol. 50
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495.
A new familial "fragile site" on chromosome 16 (q23-24). Cytogenetic and clinical considerations.
[electronic resource]
by
Shabtai, F
Klar, D
Nissimov, R
Vardimon, D
Hart, J
Halbrecht, I
Producer:
19831028
In:
Human genetics
vol. 64
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496.
Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines.
[electronic resource]
by
Kitsiou, Sofia
Kolialexi, Aggeliki
Mavrou, Ariadni
Producer:
20050414
In:
Prenatal diagnosis
vol. 24
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497.
Prevalence of autism spectrum phenomenology in Cornelia de Lange and Cri du Chat syndromes.
[electronic resource]
by
Moss, Joanna F
Oliver, Chris
Berg, Katy
Kaur, Gurmeash
Jephcott, Lesley
Cornish, Kim
Producer:
20081231
In:
American journal of mental retardation : AJMR
vol. 113
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498.
Co-segregation of Freiberg's infraction with a familial translocation t(5;7)(p13.3;p22.2) ascertained by a child with cri du chat syndrome and brachydactyly type A1B.
[electronic resource]
by
Myśliwiec, Marta
Panasiuk, Barbara
Dębiec-Rychter, Maria
Iwanowski, Piotr Sebastian
Łebkowska, Urszula
Nowakowska, Beata
Marcinkowska, Anna
Stankiewicz, Pawel
Midro, Alina T
Producer:
20150916
In:
American journal of medical genetics. Part A
vol. 167A
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499.
Growth charts for cri-du-chat syndrome: an international collaborative study.
[electronic resource]
by
Marinescu, R C
Mainardi, P C
Collins, M R
Kouahou, M
Coucourde, G
Pastore, G
Eaton-Evans, J
Overhauser, J
Producer:
20001019
In:
American journal of medical genetics
vol. 94
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500.
Transmitted deletions of medial 5p and learning difficulties; does the cadherin cluster only become penetrant when flanking genes are deleted?
[electronic resource]
by
Barber, John C K
Huang, Shuwen
Bateman, Mark S
Collins, Amanda L
Producer:
20120209
In:
American journal of medical genetics. Part A
vol. 155A
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