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TypeTitleAuthor(s)YearViews
Spread of X Inactivation on Chromosome 15 is Associated with a More Severe Phenotype in a Girl with an Unbalanced t(X;15) Translocation
Journal:
American Journal of Medical Genetics (Part A)
YEUNG, KS; Chee, WYY; Luk, HM; Kan, SYA; Tang, MHY; Lau, ETK; Shuen, AY; Lo, IFM; Chan, YK; Chung, BHY20145
 
Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care
Journal:
European Journal of Medical Genetics [Epub ahead of print]
Publisher:
Elsevier.
Liu, APY; Chow, PC; Lee, PPW; Mok, TKG; Tang, WF; Lau, ETK; Lam, STS; Chan, YK; Kan, SYA; Chau, AKT; Cheung, YF; Lau, YL; Chung, BHY201447
 
A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling
Journal:
European Journal of Medical Genetics [in-press]
Publisher:
Elsevier.
Luk, HM; Wong, VCH; Lo, IFM; Chan, YK; Lau, ETK; Kan, SYA; Tang, MHY; Tang, WF; She, WMK; Chu, WY; Sin, WK; Chung, BHY201441
 
Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong
Journal:
PLoS One
Publisher:
Public Library of Science. The Journal's web site is located at http://www.plosone.org/home.action
Kan, SYA; Lau, ETK; Tang, WF; Chan, SSY; Ding, SCK; Chan, YK; Lee, CP; Hui, PW; Chung, BHY; Leung, KY; Ma, WLT; Leung, WC; Tang, MHY201477
 
Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of Literature
Journal:
American Journal of Medical Genetics, Part A
Liu, APY; Tang, WF; Lau, ETK; Chan, YK; Kan, SYA; Wong, KY; Tso, WYW; Jalal, K; Lee, SL; Chau, CSK; Chung, BHY2013192
 
Prenatal Diagnosis of Agenesis of the Corpus Callosum and Cerebellar Vermian Hypoplasia Associated with a Microdeletion on Chromosome 1p32: Decision Minor revision
Journal:
Case Reports in Perinatal Medicine
Tang, MHY; Lau, ETK; Tan, TY; Chung, BHY; Shek, NWM201359
 
Alport's syndrome: case of a giant esophageal tumor
Journal:
Esophagus
Publisher:
Springer Japan.
Tsang, JS; Tong, DKH; Chung, BHY; Tang, MHY; Lau, ETK; Chan, GCF; Law, SYK2013159
 
22q11.2 Deletion Syndrome in Adult Chinese Patients with Conotruncal Anomalies: Dysmorphisms, Clinical Features and Underdiagnosis
Proceedings/Conference:
Hong Kong Journal of Paediatrics (New series)
Publisher:
Medcom Limited. The Journal's web site is located at http://www.hkjpaed.org/index.asp
Liu, APY; Chow, PC; Lee, PPW; Mok, TKG; Tang, WF; Lau, ETK; Lam, STS; Chan, KY; Kan, SYA; Chau, AKT; Cheung, YF; Lau, YL; Chung, BHY201382
 
Evidence of Spread of X Chromosome Inactivation On Chromosome 15 in a Girl With an Unbalanced t(X;15) Translocation
Proceedings/Conference:
Hong Kong Journal of Paediatrics (New series)
Publisher:
Medcom Limited. The Journal's web site is located at http://www.hkjpaed.org/index.asp
Yeung, KS; Chee, WYY; Luk, HM; Tang, MHY; Lau, ETK; Shuen, YA; Lo, IFM; Chan, YK; Chung, BHY201352
 
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic - a missed burden in the transition care
Proceedings/Conference:
European Journal of Human Genetics
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.nature.com/ejhg
Chung, B; Chow, P; Liu, A; Lee, P; Wong, V; Chan, K; Tang, M; Lun, KS; Lau, ETK; Cheung, YF; Chau, KT; Lau, YL201358
 
Two unusual cases of haemoglobin Bart’s hydrops fetalis due to uniparental disomy or non-paternity.
Journal:
Fetal Diagnosis and Therapy
Kou, KOT; Lee, H; Lau, B; Wong, WS; Kan, SYA; Tang, MHY; Lau, ETK; Poon, CF; Leung, KY20132
 
Update on Basic Science or Lab Technique - Array CGH for Prenatal Diagnosis
Proceedings/Conference:
Department of Obstetrics and Gynaecology, The University of Hong Kong, January 16, 2012, Hong Kong.
Lau, ETK201250
 
Disclosing results of autism genomic testing-systematic review and applying its results to clinical practice
Proceedings/Conference:
International Meeting for Autism Research, IMFAR 2012
Publisher:
International Society for Autism Research.
Chung, B; Cheuk, DKL; Tang, M; Lau, ETK; Chan, YK; Lau, YL2012144
 
Findings on Prenatal aCGH evaluation
Proceedings/Conference:
33rd Fetoscopy Working Group Meeting 2011
Lau, ETK201167
 
Evaluation of aCGH for Prenatal Diagnosis
Proceedings/Conference:
Roche Applied Science 2011 User Conference. November 3, 2011, Hong Kong.
Lau, ETK201164
 
Principle and Diagnostic pitfall of PCR and FISH
Proceedings/Conference:
HA Commissioned Training in O&G. February 28, 2011, Hong Kong.
Lau, ETK201162
 
Prenatal Diagnostic Service – Present
Proceedings/Conference:
30 years of Medical Genetics in Hong Kong. November 19, 2011, Hong Kong
Lau, ETK201161
 
Evaluation of aCGH for Prenatal Diagnosis.
Proceedings/Conference:
The 3rd Prenatal Diagnosis Conference, Quangzhou. November 5, 2011, Quangzhou, China.
Lau, ETK201156
 
Maternal serum anti-Mullerian hormone level is not superior to chronological age in predicting down syndrome pregnancies
Journal:
Prenatal Diagnosis
Publisher:
John Wiley & Sons Ltd. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/2252
Li, HWR; Hui, PW; Tang, MHY; Lau, ETK; Yeung, WSB; Ho, PC; Ng, EHY2010222
 
Confined placental mosaicism of trisomy 16 presenting with placental mass and intrauterine death
Proceedings/Conference:
The International Scientific Meeting of the International Society of Ultrasound in Obstetrics & Gynaecology
Publisher:
International Society of Ultrasound in Obstetrics & Gynaecology.
Hui, PW; Leung, KY; Lau, ETK; Tang, MHY2007102
 
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