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Standards for Dysmorphological Diagnosis in Human Fetuses.
- Published in:
- Pediatric & Developmental Pathology, 2003, v. 6, n. 5, p. 427, doi. 10.1007/s10024-003-1004-6
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- Publication type:
- Article
Third-trimester fetal MRI in isolated 10- to 12-mm ventriculomegaly: is it worth it?
- Published in:
- BJOG: An International Journal of Obstetrics & Gynaecology, 2006, v. 113, n. 8, p. 942, doi. 10.1111/j.1471-0528.2006.01003.x
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- Publication type:
- Article
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome.
- Published in:
- Clinical Genetics, 2016, v. 89, n. 5, p. 584, doi. 10.1111/cge.12720
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- Publication type:
- Article
SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects.
- Published in:
- Molecular Psychiatry, 2008, v. 13, n. 4, p. 385, doi. 10.1038/sj.mp.4002120
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- Publication type:
- Article
Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 1, p. 208, doi. 10.1002/ajmg.a.35690
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- Publication type:
- Article
Tracheal obstruction in experimental diaphragmatic hernia: an endoscopic approach in the fetal lamb.
- Published in:
- Prenatal Diagnosis, 1997, v. 17, n. 7, p. 629, doi. 10.1002/(SICI)1097-0223(199707)17:7<629::AID-PD120>3.0.CO;2-M
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- Publication type:
- Article
FETAL SERUM INTERFERON-ALPHA SUGGESTS VIRAL INFECTION AS THE AETIOLOGY OF UNEXPLAINED LATERAL CEREBRAL VENTRICULOMEGALY.
- Published in:
- Prenatal Diagnosis, 1996, v. 16, n. 10, p. 883, doi. 10.1002/(SICI)1097-0223(199610)16:10<883::AID-PD959>3.0.CO;2-5
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- Publication type:
- Article
Prenatal diagnosis of cleft lip at 11 menstrual weeks using embryoscopy in the Van der Woude syndrome.
- Published in:
- Prenatal Diagnosis, 1995, v. 15, n. 4, p. 378, doi. 10.1002/pd.1970150414
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- Publication type:
- Article
Prenatal diagnosis of tuberous sclerosis. Use of magnetic resonance imaging and its implications for prognosis.
- Published in:
- 1994
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- Publication type:
- journal article
Prenatal diagnosis of tuberous sclerosis. Use of magnetic resonance imaging and its implications for prognosis.
- Published in:
- Prenatal Diagnosis, 1994, v. 14, n. 12, p. 1151, doi. 10.1002/pd.1970141208
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- Publication type:
- Article
Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Ultrasound detection of hyaloid artery in the third trimester of pregnancy: a pathological finding.
- Published in:
- Ultrasound in Obstetrics & Gynecology, 2012, v. 39, n. 4, p. 478, doi. 10.1002/uog.10123
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- Publication type:
- Article
Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature.
- Published in:
- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 140, doi. 10.1002/pd.2167
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- Publication type:
- Article
Prenatal diagnosis of a rare skeletal dysplasia by ultrasound and scan tomography: Atelosteogenesis III (AO III). Correlation with autopsy.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 10, p. 975, doi. 10.1002/pd.2093
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- Publication type:
- Article
Prenatal Marfan syndrome: report of one case and review of the literature.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 696, doi. 10.1002/pd.1482
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- Publication type:
- Article
Prenatal rupture of a left ventricular diverticulum: a case report and review of the literature.
- Published in:
- 2004
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- Publication type:
- journal article
Prenatal diagnosis of sporadic Apert syndrome: a sequential diagnostic approach combining three-dimensional computed tomography and molecular biology.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Expression of the Sonic hedgehog (SHH) gene during early human development and phenotypic expression of new mutations causing holoprosencephaly.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 9, p. 1683, doi. 10.1093/hmg/8.9.1683
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- Publication type:
- Article
C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome.
- Published in:
- Cytogenetic & Genome Research, 2006, v. 112, n. 1/2, p. 16, doi. 10.1159/000087509
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- Publication type:
- Article
The Distribution of SMN Protein Complex in Human Fetal Tissues and Its Alteration in Spinal Muscular Atrophy.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 12, p. 1927, doi. 10.1093/hmg/7.12.1927
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- Publication type:
- Article
The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 12, p. 1927, doi. 10.1093/hmg/7.12.1927
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- Publication type:
- Article
Missense FGFR3 Mutations Create Cysteine Residues in Thanatophoric Dwarfism Type I (TD1).
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 4, p. 509, doi. 10.1093/hmg/5.4.509
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- Publication type:
- Article