Detalles de la búsqueda
1.
Prenatal Ultrasound Evaluation and Outcome of Pregnancy with Fetal Cystic Hygromas and Lymphangiomas.
J Med Ultrasound
; 25(1): 12-15, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-30065449
2.
Reply to Comment on An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus.
J Med Ultrasound
; 26(3): 170, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30283208
3.
Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report.
Taiwan J Obstet Gynecol
; 62(2): 334-335, 2023 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-36965904
4.
An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus.
J Med Ultrasound
; 25(3): 188-189, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-30065489
5.
An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus.
J Med Ultrasound
; 25(4): 255-257, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-30065504
6.
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
Taiwan J Obstet Gynecol
; 57(5): 739-744, 2018 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-30342663
7.
Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3.
Taiwan J Obstet Gynecol
; 56(1): 87-92, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-28254233
8.
Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay.
Taiwan J Obstet Gynecol
; 56(1): 93-97, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-28254235
9.
Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder.
Taiwan J Obstet Gynecol
; 56(1): 98-101, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-28254236
10.
Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.
Taiwan J Obstet Gynecol
; 56(3): 398-401, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28600059
11.
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome.
Taiwan J Obstet Gynecol
; 56(2): 238-242, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-28420516
12.
Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.
Taiwan J Obstet Gynecol
; 56(1): 102-105, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-28254208
13.
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.
Taiwan J Obstet Gynecol
; 56(4): 554-557, 2017 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-28805618
14.
Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
Taiwan J Obstet Gynecol
; 56(2): 217-223, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-28420511
15.
Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis.
Taiwan J Obstet Gynecol
; 56(2): 230-233, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-28420514
16.
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2.
Taiwan J Obstet Gynecol
; 56(2): 234-237, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-28420515
17.
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22âq11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability.
Taiwan J Obstet Gynecol
; 55(6): 856-860, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28040133
18.
Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality.
Taiwan J Obstet Gynecol
; 55(6): 871-873, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28040137
19.
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion.
Taiwan J Obstet Gynecol
; 55(1): 117-20, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26927262
20.
Prenatal diagnosis of partial monosomy 5p (5p15.1âpter) and partial trisomy 7p (7p15.2âpter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.
Taiwan J Obstet Gynecol
; 55(4): 591-5, 2016 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-27590389