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Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Direct transmission of the 18q- syndrome from mother to daughterC P Chen, S P Lin, S R Chern, et al.
Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.
Prenatal Diagnosis|November 25, 1998
Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequenceC P Chen, S R Chern, C C Lee, et al.
Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXYC P Chen, S R Chern, C L Chang, et al.
Prenatal Diagnosis|March 10, 2001
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasiaC P Chen, S R Chern, J C Shih, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delayC P Chen, S P Lin, S R Chern, et al.
Prenatal Diagnosis|April 5, 2001
Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial cleftsC P Chen, S R Chern, C Y Tzen, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disabilityC-P Chen, S-P Lin, S-R Chern, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delayC-P Chen, S-P Lin, Y-N Su, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Pure distal 9p deletion in a female infant with cerebral palsyC-P Chen, S-P Lin, Y-N Su, et al.
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