Lin SP - Search Results

1

Perinatal findings in a male fetus with congenital megacystis and anorectal malformations.

Chen CP, Wang W, Lin SP, Sheu JC, Tsai JD. Chen CP, et al. Among authors: lin sp. Fetal Diagn Ther. 1998 Nov-Dec;13(6):348-51. doi: 10.1159/000020867. Fetal Diagn Ther. 1998. PMID: 9933817

2

Favorable outcome in a fetus with an early-onset extensive cystic hygroma colli and intralesional hemorrhage.

Chen CP, Wang W, Lin SP, Sheu JC, Tzen CY. Chen CP, et al. Among authors: lin sp. Am J Perinatol. 1998;15(11):601-5. doi: 10.1055/s-2007-994077. Am J Perinatol. 1998. PMID: 10064200

3

Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.

Chen CP, Devriendt K, Chern SR, Lee CC, Wang W, Lin SP. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2000 May;20(5):384-9. Prenat Diagn. 2000. PMID: 10820405

4

Distal 10q trisomy associated with bilateral hydronephrosis in infancy.

Chen CP, Lin SP. Chen CP, et al. Among authors: lin sp. Genet Couns. 2003;14(3):359-62. Genet Couns. 2003. PMID: 14577683

5

De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.

Chen CP, Lin SP, Chern SR, Lee CC, Huang JK, Wang W, Liao YW. Chen CP, et al. Among authors: lin sp. Genet Couns. 2004;15(4):437-42. Genet Couns. 2004. PMID: 15658619

6

Direct transmission of the 18q- syndrome from mother to daughter.

Chen CP, Lin SP, Chern SR, Lee CC, Huang JK, Wang W. Chen CP, et al. Among authors: lin sp. Genet Couns. 2006;17(2):185-9. Genet Couns. 2006. PMID: 16970036

7

Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.

Chen CP, Lin SP, Lee CC, Town DD, Wang W. Chen CP, et al. Among authors: lin sp. Genet Couns. 2006;17(3):301-6. Genet Couns. 2006. PMID: 17100198

8

Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.

Chen CP, Liu FF, Jan SW, Lin SP, Lan CC. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 1996 Mar;16(3):270-5. doi: 10.1002/(SICI)1097-0223(199603)16:3<270::AID-PD836>3.0.CO;2-0. Prenat Diagn. 1996. PMID: 8710784

9

Progressive fetal axillary cystic lymphangioma with coexistent naevus flammeus.

Chen CP, Chen HC, Liu FF, Jan SW, Lin SP, Sheu JC, Chen BF. Chen CP, et al. Among authors: lin sp. Br J Dermatol. 1997 Jan;136(1):102-4. Br J Dermatol. 1997. PMID: 9039304

10

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).

Chen CP, Lin CC, Chuang CY, Lee CC, Chen WL, Jan SW, Lin SP. Chen CP, et al. Among authors: lin sp, lin cc. Prenat Diagn. 1997 Jul;17(7):675-80. doi: 10.1002/(sici)1097-0223(199707)17:7<675::aid-pd114>3.0.co;2-0. Prenat Diagn. 1997. PMID: 9249870

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