[[abstract]]We report an 18-gestational-week fetus with oligohydramnios, orofacial clefting, bilateral multicystic kidneys and the Dandy-Walker malformation. Characteristic craniofacial features include a turricephalic prominent forehead, hypertelorism, low-set ears, a flat nasal bridge, mid-face hypoplasia, bilateral cleft lip and palate, and a thick nuchal fold. Array-comparative genomic hybridization (CGH) analysis demonstrated a 12Mb deletion of 6p24.1-->pter
Popliteal pterygium syndrome (PPS) is an extremely rare autosomal dominant disorder, characterized b...
WOS: 000337197200007PubMed ID: 24032288Partial trisomy 2p24 -> pter and monosomy 18q22.1 -> qter res...
21st European Congress of Perinatal Medicine -- SEP 10-13, 2008 -- Istanbul, TURKEYGoldston syndrome...
[[abstract]]We report an 18-gestational-week fetus with oligohydramnios, orofacial clefting, bilater...
[[abstract]]Objective We present prenatal diagnosis of an interstitial 8q22.2-q23.3 deletion associa...
Objective To present the prenatal diagnosis and molecular cytogenetic characterization of de novo pa...
[[abstract]]Patients with partial trisomy 3p seldom present major dysmorphic features, and holoprose...
Clinical reports of cases with deletions in chromosome 6p are relatively rare. We present a detailed...
Objective: To present prenatal diagnosis and molecular cytogenetic characterization of de nova parti...
A female fetus with an unusual collection of congenital anomalies was detected prenatally. The pregn...
[[abstract]]"Objective To present the prenatal diagnosis and molecular cytogenetic characterization ...
BACKGROUND: Ectrodactyly-ectodermal dysplasia-clefting syndrome 3 (EEC) is one of the six overlappin...
Patients with partial trisomy 3p seldom present major dysmorphic features, and holoprosencephaly occ...
Patients with partial trisomy 3p seldom present major dysmorphic features, and holoprosencephaly occ...
We report a patient with severe developmental delay, failure to thrive, microbrachycephaly, large an...
Popliteal pterygium syndrome (PPS) is an extremely rare autosomal dominant disorder, characterized b...
WOS: 000337197200007PubMed ID: 24032288Partial trisomy 2p24 -> pter and monosomy 18q22.1 -> qter res...
21st European Congress of Perinatal Medicine -- SEP 10-13, 2008 -- Istanbul, TURKEYGoldston syndrome...
[[abstract]]We report an 18-gestational-week fetus with oligohydramnios, orofacial clefting, bilater...
[[abstract]]Objective We present prenatal diagnosis of an interstitial 8q22.2-q23.3 deletion associa...
Objective To present the prenatal diagnosis and molecular cytogenetic characterization of de novo pa...
[[abstract]]Patients with partial trisomy 3p seldom present major dysmorphic features, and holoprose...
Clinical reports of cases with deletions in chromosome 6p are relatively rare. We present a detailed...
Objective: To present prenatal diagnosis and molecular cytogenetic characterization of de nova parti...
A female fetus with an unusual collection of congenital anomalies was detected prenatally. The pregn...
[[abstract]]"Objective To present the prenatal diagnosis and molecular cytogenetic characterization ...
BACKGROUND: Ectrodactyly-ectodermal dysplasia-clefting syndrome 3 (EEC) is one of the six overlappin...
Patients with partial trisomy 3p seldom present major dysmorphic features, and holoprosencephaly occ...
Patients with partial trisomy 3p seldom present major dysmorphic features, and holoprosencephaly occ...
We report a patient with severe developmental delay, failure to thrive, microbrachycephaly, large an...
Popliteal pterygium syndrome (PPS) is an extremely rare autosomal dominant disorder, characterized b...
WOS: 000337197200007PubMed ID: 24032288Partial trisomy 2p24 -> pter and monosomy 18q22.1 -> qter res...
21st European Congress of Perinatal Medicine -- SEP 10-13, 2008 -- Istanbul, TURKEYGoldston syndrome...