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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.
HLA|January 20, 2017
A dispermic chimerism detected in a Taiwanese potential unrelated hematopoietic stem cell donorE K L Yang, S G E Marsh, P-Y Chen, et al.
Changgeng Yi Xue Za Zhi|December 1, 1992
[Implementation of stereotactic focal radiotherapy using 10 MV x-ray]C P Tu, F J Lin, J A Liang, et al.
Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)C P Chen, C C Lin, C Y Chuang, et al.
Prenatal Diagnosis|June 1, 1997
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive resultsC P Chen, S R Chern, F F Liu, et al.
The British Journal of Dermatology|February 1, 1997
Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascitesC P Chen, H C Chen, F F Liu, et al.
The British Journal of Dermatology|January 1, 1997
Progressive fetal axillary cystic lymphangioma with coexistent naevus flammeusC P Chen, H C Chen, F F Liu, et al.
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