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Sts Lam

Observed names: Lam, STS, STS LAM, STS Lam
OpenAlex ID: A5111999334
Spontaneous growth in Chinese patients with Turner's syndrome and influence of karyotype
1997 · LCK Low, C Sham, et al. · Acta Paediatrica · 20
Detection of resistance to thyroid hormone by cord blood screening
1995 · GWK Wong, CC Shek, et al. · Acta Paediatrica · 13
Central diabetes insipidus in a newborn with deletion of chromosome 7q
1997 · PC NG, CH LEE, et al. · Journal of Paediatrics and Child Health · 10
Thanatophoric Dysplasia Type 1 (TD1) without "Telephone Receivers"
2006 · Acf Lam, Yy Lam, et al. · 8
Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome
2006 · Acf Lam, Kks Lai, et al. · 4
Pseudohypoparathyroidism Type 1b: First Case Report in Chinese and Literature Review
2015 · HM Luk, Sts Lam · 3
A Case of Perinatal Lethal Form of Hypophosphatasia; and Review of Literatures
2006 · Acf Lam, CW Lam, et al. · 3
Subtelomeric 1q deletion syndrome causing patella hypoplasia and limb deformities, features overlapping with genitopatellar syndrome
2009 · ACF Lam, KKS Lai, et al. · Clinical Genetics · 2
Thanatophoric Dysplasia Variant, San Diego Type in a Chinese Fetus, Caused by C746G Missense Mutation in FGFR3 Gene
2006 · Acf Lam, T.F. Tong, et al. · The HKU Scholars Hub (University of Hong Kong) · 2
Phenotypic Spectrum of 3 Pseudohypoparathyroidism type 1a, and 2 Pseudopseudohypoparathyroidism Chinese Patients with Novel GNAS Mutations
2006 · Acf Lam, Sts Lam · 2
A Clinical and Molecular Study of 51 Chinese Families with Noonan Syndrome
2006 · D. K. L. Chan, Sts Lam · 2
Craniofrontonasal Dysplasia: A Report of Two Chinese Families and Literature Review
2015 · HM Luk, Sts Lam · 1
Boomerang Dysplasia in a Chinese Female Fetus
2006 · Acf Lam, Sj Hu, et al. · 1
Chinese patients with rasopathies: Detection of 29 known and novel variants using next-generation sequencing (NGS)
2015 · KC Leung, Ivan F. M. Lo, et al.
NSD1+/- DNA methylation (DNAm) signature: A novel functional diagnostic tool for Sotos syndrome
2014 · S Chonufani, Cheryl Cytrynbaum, et al.
Identifying genetic mutations in patients with rasopathies using a next generation sequencing diagnostic pipeline in Hong Kong
2014 · Ifm Lo, KC Leung, et al.
Massive parallel sequencing for the genetic diagnosis of rasopathies: a study of 58 Chinese patients in Hong Kong
2013 · Ifm Lo, KC Leung, et al.
22q11.2 deletion syndrome in adult Chinese Patients with Conotruncal Anomalies: dysmorphisms, clinical features and underdiagnosis
2013 · Apy Liu, PC Chow, et al.
Two Chinese Patients with Loeys-Dietz Syndrome: A Connecitve Tissue Disorder with Marfan-like Features and Vasculopathy
2012 · Cca Ho, Stephen Chan, et al. · The HKU Scholars Hub (University of Hong Kong)
ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
2011 · Assunta CH Ho, Joannie Hui, et al. · Pediatric Rheumatology
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Two cases of spondylothoracic dysostosis (Jarcho Levin syndrome) in Chinese population
2011 · Cws Lai, Ewl Lau, et al.
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes (oral presentation)
2007 · Bhy Chung, Sts Lam, et al. · The HKU Scholars Hub (University of Hong Kong)
Identification of 7 novel TGFBR2 (Transforming Growth Factor-Beta Receptor 2) mutations in Chinese with Marfan syndrome (MFS) and related phenotypes using denaturing high performance liquid chromatography (DHPLC)
2007 · Bhy Chung, Li Yh, et al. · The HKU Scholars Hub (University of Hong Kong)
Identification of 7 novel TGFBR2 mutations in Chinese with marfan syndrome (MFS) and related phenotypes using DHPLC
2007 · Bhy Chung, Li Yh, et al.
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes
2006 · Bhy Chung, Sts Lam, et al. · The HKU Scholars Hub (University of Hong Kong)
Works count: 31
Citation count: 71
H-index: 4
I10-index: 3
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