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Items: 1 to 20 of 740

1.

Integrated analysis of the critical region 5p15.3-p15.2 associated with cri-du-chat syndrome.

Corrêa T, Feltes BC, Riegel M.

Genet Mol Biol. 2019 Apr 11. pii: S1415-47572019005013103. doi: 10.1590/1678-4685-GMB-2018-0173. [Epub ahead of print]

2.

Improved memory and reduced anxiety in δ-catenin transgenic mice.

Ryu T, Park HJ, Kim H, Cho YC, Kim BC, Jo J, Seo YW, Choi WS, Kim K.

Exp Neurol. 2019 Apr 11. pii: S0014-4886(19)30067-6. doi: 10.1016/j.expneurol.2019.04.006. [Epub ahead of print]

PMID:
30981806
3.

Age-related Behavioural Change in Cornelia de Lange and Cri du Chat Syndromes: A Seven Year Follow-up Study.

Cochran L, Welham A, Oliver C, Arshad A, Moss JF.

J Autism Dev Disord. 2019 Apr 2. doi: 10.1007/s10803-019-03966-6. [Epub ahead of print]

PMID:
30941551
4.

Prenatal diagnosis of 5p deletion syndrome: Report of five cases.

Mak ASL, Ma TWL, Chan KYK, Kan ASY, Tang MHY, Leung KY.

J Obstet Gynaecol Res. 2019 Apr;45(4):923-926. doi: 10.1111/jog.13911.

PMID:
30932301
5.

Children and adults affected by Cri du Chat syndrome: Care's recommendations.

Liverani ME, Spano A, Danesino C, Malacarne M, Cavani S, Spunton M, Guala A.

Pediatr Rep. 2019 Feb 26;11(1):7839. doi: 10.4081/pr.2019.7839. eCollection 2019 Feb 26.

6.

Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.

Liang D, Cram DS, Tan H, Linpeng S, Liu Y, Sun H, Zhang Y, Tian F, Zhu H, Xu M, Wang H, Yu F, Wu L.

Genet Med. 2019 Mar 4. doi: 10.1038/s41436-019-0467-4. [Epub ahead of print]

PMID:
30828085
7.

Management of Self-injurious Behaviors in Children with Neurodevelopmental Disorders: A Pharmacotherapy Overview.

Sabus A, Feinstein J, Romani P, Goldson E, Blackmer A.

Pharmacotherapy. 2019 Feb 22. doi: 10.1002/phar.2238. [Epub ahead of print]

PMID:
30793794
8.

Generation of induced pluripotent stem cells (iPSCs) from patient with Cri du Chat Syndrome.

Piovani G, Lanzi G, Ferraro RM, Masneri S, Barisani C, Savio G, Giliani SC.

Stem Cell Res. 2019 Mar;35:101393. doi: 10.1016/j.scr.2019.101393. Epub 2019 Jan 26.

9.

Difficult airway management and suspected malignant hyperthermia in a Child with Cri Du Chat Syndrome.

Amata AO.

Saudi J Anaesth. 2019 Jan-Mar;13(1):81-83. doi: 10.4103/sja.SJA_304_18. No abstract available.

10.

Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report.

Vado Y, Errea-Dorronsoro J, Llano-Rivas I, Gorria N, Pereda A, Gener B, Garcia-Naveda L, Perez de Nanclares G.

BMC Med Genomics. 2018 Dec 27;11(1):124. doi: 10.1186/s12920-018-0441-z.

11.

Prenatal sonographic diagnosis of isolated fetal ascites in cri-du-chat (5p-) syndrome: A case report.

Cardoso MC, Raposo MI, Ormonde M, Monteiro R, Sampaio A, Cosme P, Mota-Vieira L.

J Clin Ultrasound. 2019 May;47(4):232-234. doi: 10.1002/jcu.22679. Epub 2018 Dec 4.

PMID:
30511740
12.

Prenatal Diagnosis of BACs-on-Beads Assay in 3647 Cases of Amniotic Fluid Cells.

Li C, Chen B, Zheng J, Cheng L, Song T, Guo F, Xu H, Yan F, Xu Y, Li Y, Zhang J.

Reprod Sci. 2018 Oct 16:1933719118804416. doi: 10.1177/1933719118804416. [Epub ahead of print]

PMID:
30326779
13.

The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort.

Sanders CD, Leigh MW, Chao KC, Weck KE, King I, Wolf WE, Campbell DJ, Knowles MR, Zariwala MA, Shapiro AJ.

Pediatr Pulmonol. 2018 Nov;53(11):1565-1573. doi: 10.1002/ppul.24159. Epub 2018 Sep 20.

PMID:
30238669
14.

[Cri-du-chat syndrome in neonatal period].

Bai MM, Meng L, Li W.

Zhonghua Er Ke Za Zhi. 2018 Jul 2;56(7):554. doi: 10.3760/cma.j.issn.0578-1310.2018.07.018. Chinese. No abstract available.

PMID:
29996194
15.

Effects of Oral Stimulation Intervention in Newborn Babies with Cri du Chat Syndrome: Single-Subject Research Design.

Kim MK, Kim DJ.

Occup Ther Int. 2018 May 8;2018:6573508. doi: 10.1155/2018/6573508. eCollection 2018.

16.

Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent in situ hybridization.

Eswarachari V, Kadam P, Movva S, Lingaiah S, Akther RM, Kidangan FX, Gowda KC, Golakoti RRK, Lall M, Mahajan S, Saviour P, Puri R, Verma IC, Vedam RL.

J Matern Fetal Neonatal Med. 2018 Jun 13:1-4. doi: 10.1080/14767058.2018.1481383. [Epub ahead of print]

PMID:
29793366
17.

Novel ocular findings with 5p deletion and partial trisomy of distal 4q.

Lin S, Rawlins L, Turner C, Doyle E, Sleep T.

Can J Ophthalmol. 2018 Jun;53(3):e89-e90. doi: 10.1016/j.jcjo.2017.09.010. Epub 2017 Oct 27. No abstract available.

PMID:
29784183
18.

Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.

Yokoyama E, Del Castillo V, Sánchez S, Ramos S, Molina B, Torres L, Navarro MJ, Avila S, Castrillo JL, García-De Teresa B, Asch B, Frías S.

Mol Cytogenet. 2018 May 9;11:30. doi: 10.1186/s13039-018-0374-4. eCollection 2018.

19.

Mental Health and Well-Being in Mothers of Children With Rare Genetic Syndromes Showing Chronic Challenging Behavior: A Cross-Sectional and Longitudinal Study.

Adams D, Clarke S, Griffith G, Howlin P, Moss J, Petty J, Tunnicliffe P, Oliver C.

Am J Intellect Dev Disabil. 2018 May;123(3):241-253. doi: 10.1352/1944-7558-123.3.241.

PMID:
29671635
20.

Cri Du Chat Syndrome.

Ajitkumar A, Mathai JK.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2019 Jan-.
2019 Feb 22.

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