Works matching DE "XYY syndrome"

Results: 39

Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literature.

Published in:

European Journal of Pediatrics, 2014, v. 173, n. 3, p. 277, doi. 10.1007/s00431-014-2267-9

By:

Margari, Lucia;
Lamanna, Anna;
Craig, Francesco;
Simone, Marta;
Gentile, Mattia

Publication type:

Article

Sensory Features as a Marker of Autism Spectrum Disorders.

Published in:

Journal of Autism & Developmental Disorders, 2020, v. 50, n. 6, p. 2240, doi. 10.1007/s10803-019-03948-8

By:

Bizzell, Ebonee;
Ross, Judith;
Rosenthal, Carly;
Dumont, Rachel;
Schaaf, Roseann

Publication type:

Article

Preverbal skills in 8-month-old children with sex chromosome trisomies.

Published in:

First Language, 2021, v. 41, n. 2, p. 200, doi. 10.1177/0142723720962944

By:

Zampini, Laura;
Burla, Tiziana;
Silibello, Gaia;
Capelli, Elena;
Dall'Ara, Francesca;
Rigamonti, Claudia;
Ajmone, Paola Francesca;
Monti, Federico;
Zanchi, Paola;
Lalatta, Faustina;
Costantino, Maria Antonella;
Vizziello, Paola Giovanna

Publication type:

Article

Multifocal dysembryoplastic neuroepithelial tumour in a male with the XYY syndrome.

Published in:

Neuropathology & Applied Neurobiology, 2005, v. 31, n. 5, p. 556, doi. 10.1111/j.1365-2990.2005.00680.x

By:

Krossnes, B. K.;
Wester, K.;
Moen, G.;
Mørk, S. J.

Publication type:

Article

Skeletal and dental abnormalities in patients with sex chromosome aberrations: a systematic case-based review.

Published in:

Polish Journal of Pediatrics / Pediatria Polska, 2022, v. 97, n. 1, p. 29, doi. 10.5114/polp.2022.114705

By:

Gruszczyński, Dawid;
Nijakowski, Kacper;
Wolska-Bułach, Anna;
Lacka, Katarzyna

Publication type:

Article

A unique association of Noonan syndrome and 47,XYY syndrome in a male presenting with failure to thrive.

Published in:

2017

By:

Bellfield, Edward J.;
Shad, Zohra

Publication type:

Case Study

47,XYY Syndrome and Male Infertility.

Published in:

Reviews in Urology, 2013, v. 15, n. 4, p. 188, doi. 10.3909/riu0580]

By:

Ina W. Kim;
Khadilkar, Arjun C.;
Ko, Edmund Y.;
Sabanegh. Jr, Edmund S.

Publication type:

Article

Reaction to Diagnosis and Parental Concerns in Parents of Children and Young Adults With XYY Syndrome.

Published in:

Child: Care, Health & Development, 2024, v. 50, n. 5, p. 1, doi. 10.1111/cch.13324

By:

Zampini, Laura;
Zanchi, Paola;
Silibello, Gaia;
Mastromattei, Domenica;
Ajmone, Paola Francesca;
Dall'Ara, Francesca;
Monti, Federico;
Costantino, Maria Antonella;
Vizziello, Paola Giovanna

Publication type:

Article

Spontaneous resolution of cystic hygroma in 47,XYY fetus.

Published in:

2007

By:

Phupong, Vorapong;
Sittisomwong, Tul

Publication type:

journal article

Associated medical disorders and disabilities in children with autistic disorders.

Published in:

Autism: The International Journal of Research & Practice, 2004, v. 8, n. 1, p. 49, doi. 10.1177/1362361304040638

By:

Kielinen, Marko;
Rantala, Heikki;
Timonen, Eija;
Linna, Sirkka-Liisa;
Moilanen, Irma

Publication type:

Article

Myotonic dystrophy associated with 47 XYY syndrome.

Published in:

2000

By:

Asano, Atsutoshi;
Motomura, Naoyasu;
Yokota, Shingo;
Yoneda, Hiroshi;
Sakai, Toshiaki;
Tsutsumi, Shigetoshi

Publication type:

Case Study

Aneuploidy in Human Spermatozoa.

Published in:

Cytogenetic & Genome Research, 2011, v. 133, n. 2-4, p. 91, doi. 10.1159/000323795

By:

Templado, C.;
Vidal, F.;
Estop, A.

Publication type:

Article

Chromosomal abnormality: Prevalence, prenatal diagnosis and associated anomalies based on a provincial‐wide birth defects monitoring system.

Published in:

Journal of Obstetrics & Gynaecology Research, 2021, v. 47, n. 3, p. 865, doi. 10.1111/jog.14569

By:

Xie, Donghua;
Yang, Wenzhen;
Fang, Junqun;
Li, Haoxian;
Xiong, Lili;
Kong, Fanjuan;
Wang, Aihua;
Liu, Zhiyu;
Wang, Hua

Publication type:

Article

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.

Published in:

Journal of Intellectual Disability Research, 1998, v. 42, n. 1, p. 8, doi. 10.1046/j.1365-2788.1998.00091.x

By:

Weidmer-Mikhail;
Sheldon;
Ghaziuddin;
Mikhail, E. Weidmer

Publication type:

Article

Prader-Willi syndrome in a child with XYY.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 6, p. 412, doi. 10.1007/s100380050189

By:

Honma, A.;
Ishii, R.;
Ito, A.;
Kato, M.;
Saitoh, S.;
Hayasaka, K.

Publication type:

Article

Possible contribution of XYY syndrome to neuroleptic malignant syndrome in a child receiving quetiapine.

Published in:

American Journal of Health-System Pharmacy, 2010, v. 67, n. 6, p. 459, doi. 10.2146/ajhp090091

By:

Randolph, Timothy C.

Publication type:

Article

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Published in:

Developmental Medicine & Child Neurology, 2014, v. 56, n. 4, p. 346, doi. 10.1111/dmcn.12294

By:

Simpson, Nuala H;
Addis, Laura;
Brandler, William M;
Slonims, Vicky;
Clark, Ann;
Watson, Jocelynne;
Scerri, Thomas S;
Hennessy, Elizabeth R;
Bolton, Patrick F;
Conti‐Ramsden, Gina;
Fairfax, Benjamin P;
Knight, Julian C;
Stein, John;
Talcott, Joel B;
O'Hare, Anne;
Baird, Gillian;
Paracchini, Silvia;
Fisher, Simon E;
Newbury, Dianne F;
Consortium, SLI

Publication type:

Article

Sex chromosomes and the brain: a study of neuroanatomy in XYY syndrome.

Published in:

Developmental Medicine & Child Neurology, 2012, v. 54, n. 12, p. 1149, doi. 10.1111/j.1469-8749.2012.04418.x

By:

BRYANT, DANIEL M;
HOEFT, FUMIKO;
LAI, SONG;
LACKEY, JOHN;
ROELTGEN, DAVID;
ROSS, JUDITH;
REISS, ALLAN L

Publication type:

Article

Stimulant medication in 47,XYY syndrome: a report of two cases.

Published in:

2005

By:

Anne Ruud;
Peter Arnesen;
Liv Larsen Stray;
Stéphane Vildalen;
Per Vesterhus

Publication type:

Case Study

Prenatal Diagnosis of Sex Chromosome Abnormalities: The 8-Year Experience of a Single Medical Center.

Published in:

Fetal Diagnosis & Therapy, 2008, v. 23, n. 1, p. 76, doi. 10.1159/000109231

By:

Vaknin, Zvi;
Reish, Orit;
Ben-Ami, Ido;
Heyman, Eli;
Herman, Arie;
Maymon, Ron

Publication type:

Article

Nonmosaic 47,XYY syndrome presenting with male infertility: case series.

Published in:

Andrologia, 2012, v. 44, n. 3, p. 200, doi. 10.1111/j.1439-0272.2010.01129.x

By:

Abdel-Razic, M. M.;
Abdel-Hamid, I. A.;
ElSobky, E. S.

Publication type:

Article

Primary male infertility in Kuwait: a cytogenetic and molecular study of 289 infertile Kuwaiti patients.

Published in:

Andrologia, 2007, v. 39, n. 3, p. 87, doi. 10.1111/j.1439-0272.2007.00769.x

By:

Mohammed, F.;
Al-Yatama, F.;
Al-Bader, M.;
Tayel, S. M.;
Gouda, S.;
Naguib, K. K.

Publication type:

Article

Apparent Homozygosity for a gr/gr AZFc Deletion in A 47,XYY Man with Oligozoospermia and Secondary Infertility.

Published in:

Journal of Reproduction & Infertility, 2022, p. 296, doi. 10.18502/jri.v23i4.10816

By:

Bunyan, David J.;
Saran, Mili;
Hobbs, James I.;
Anderson, David J.;
Duncan-Flavell, Philippa J.;
Howarth, Rachel J;
Callaway, Jonathan L. A.;
MacPherson, James N.

Publication type:

Article

Reply to Herlihy and Halliday.

Published in:

2008

By:

Morris, Joan

Publication type:

Letter

XYY syndrome: a 13-year-old boy with tall stature.

Published in:

2015

By:

Won Ha Jo;
Mo Kyung Jung;
Ki Eun Kim;
Hyun Wook Chae;
Duk Hee Kim;
Ah Reum Kwon;
Ho-Seong Kim

Publication type:

Case Study

An infertile case of 47,XYY syndrome without autistic spectrum: Cost effective well-define of extra Y chromosome by GTG, C bandings, QF-PCR and FISH analyses.

Published in:

2016

By:

Özdemir, Özturk;
Paksoy, Barış;
Gürgen, Atilla;
Oruç, Mine;
Yıldız, Onur;
Uysal, Diğdem;
Uludağ, Ahmet;
Silan, Fatma

Publication type:

Case Study

Asperger’s Disorder in an Adolescent With 47,XYY Chromosomal Syndrome.

Published in:

Clinical Pediatrics, 2011, v. 50, n. 6, p. 562, doi. 10.1177/0009922810380453

By:

Cashion, Larry;
Van Roden, Angela

Publication type:

Article

Pregnancies with positive non-invasive prenatal testing result for sex chromosome abnormalities in a tertiary hospital in Hong Kong.

Published in:

Hong Kong Journal of Gynaecology, Obstetrics & Midwifery, 2022, v. 22, n. 2, p. 87, doi. 10.12809/hkjgom.22.2.07

By:

SO, P. L.;
Lai, S.;
WONG, P. P.;
SIONG, K. H.;
LEUNG, H. K.;
SIN, W. K.;
KAN, Anita S. Y.;
LUK, H. M.;
LO, Ivan F. M.;
YEUNG, K. C. A. U.;
WONG, S. F.

Publication type:

Article

Diagnostic challenges of Marfan syndrome in an XYY young man.

Published in:

2012

By:

Lebreiro, Ana;
Martins, Elisabete;
Machado, José Carlos;
Abreu-Lima, Cassiano

Publication type:

Case Study

A patient with 46,XY/47,XYY karyotype and female phenotype: a case report.

Published in:

BMC Endocrine Disorders, 2020, v. 20, n. 1, p. 1, doi. 10.1186/s12902-020-0523-8

By:

Liu, Zhi-Hui;
Zhou, Shi-Chao;
Du, Jun-Wen;
Zhang, Kun;
Wu, Tao

Publication type:

Article

PHYSIQUE IN CHROMOSOMAL DISORDERS.

Published in:

Papers on Anthropology, 2006, v. 15, p. 28

By:

Buday, József

Publication type:

Article

Association Between Venous Leg Ulcers and Sex Chromosome Anomalies in Men.

Published in:

Acta Dermato-Venereologica, 2010, v. 90, n. 6, p. 612, doi. 10.2340/00015555-0949

By:

Gattringer, Cornelia;
Scheurecker, Christine;
Höpfl, Reinhard;
Müller, Hansgeorg

Publication type:

Article

Double Aneuploidy: A Case of Trisomy 21 with XYY.

Published in:

European Journal of General Medicine, 2011, v. 8, n. 4, p. 338, doi. 10.29333/ejgm/82767

By:

K”ken, Resit;
Bklmez, Aysegul;
Nadirgil K”ken, Glengl;
Eser, Betl;
Samlı, Hale;
Demir, Tevfik;
Solak, Mustafa

Publication type:

Article

The XYY Story as a Cautionary Tale: How Scientific Misinformation and Common Biases Can Negatively Impact Lives and Opinions.

Published in:

AMWA Journal: American Medical Writers Association Journal, 2024, v. 39, n. 4, p. 40, doi. 10.55752/amwa.2024.393

By:

Ebeling, Helena I.;
Beckwith, Jonathan R.

Publication type:

Article

Displasia ectodérmica hipohidrótica autosómica dominante. Reporte de un caso.

Published in:

2012

By:

Triviño F., Loreto;
Avaria E., Jaime;
Vargas F., María José;
Alarcón C., Rosario

Publication type:

Case Study

Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report.

Published in:

2011

By:

Liao, Can;
Fu, Fang;
Zhang, Liang

Publication type:

journal article

Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia.

Published in:

Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-016-0218-z

By:

Caiyun Wu;
Liu Wang;
Furhan Iqbal;
Xiaohua Jiang;
Ihtisham Bukhari;
Tonghang Guo;
Gengxin Yin;
Cooke, Howard J.;
Zhenyi Cao;
Hong Jiang;
Qinghua Shi

Publication type:

Article

THE XYY OFFENDER: A MODERN MYTH?

Published in:

Journal of Criminal Law, Criminology & Police Science, 1971, v. 62, n. 1, p. 59, doi. 10.2307/1142122

By:

Fox, Richard G.

Publication type:

Article

Diagnosis and mortality in 47,XYY persons: a registry study.

Published in:

Orphanet Journal of Rare Diseases, 2010, v. 5, p. 15, doi. 10.1186/1750-1172-5-15

By:

Stochholm, Kirstine;
Juul, Svend;
Gravholt, Claus H.

Publication type:

Article