Found: 23
Select item for more details and to access through your institution.
Ovotesticular Disorder of Sex Development (Ovotestis) in Simpson–Golabi–Behmel Syndrome: Expansion of the Clinical Spectrum.
- Published in:
- Pediatric & Developmental Pathology, 2019, v. 22, n. 1, p. 70, doi. 10.1177/1093526618770327
- By:
- Publication type:
- Article
Lethal Hypoplasia and Developmental Anomalies of the Lungs in a Newborn with Intrauterine Adrenal Hemorrhage and Cerebral Infarcts: A Proposed Pulmonary Disruption Sequence.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Utility of Fetal Karyotype in the Evaluation of Phenotypically Abnormal Stillbirths.
- Published in:
- Pediatric & Developmental Pathology, 2009, v. 12, n. 3, p. 217, doi. 10.2350/07-07-0307.1
- By:
- Publication type:
- Article
Effects of Chemotherapy during Pregnancy on the Placenta.
- Published in:
- Pediatric & Developmental Pathology, 2009, v. 12, n. 1, p. 35, doi. 10.2350/08-03-0435.1
- By:
- Publication type:
- Article
Activin Subunit and Receptor Expression in Normal and Cleft Human Fetal Palate Tissues.
- Published in:
- Pediatric & Developmental Pathology, 2007, v. 10, n. 6, p. 436, doi. 10.2350/06-05-0087.1
- By:
- Publication type:
- Article
Second-Trimester Maternal Serum Markers in Twin Pregnancy With Complete Mole: Report of 2 Cases.
- Published in:
- Pediatric & Developmental Pathology, 2005, v. 8, n. 2, p. 230, doi. 10.1007/s10024-005-0121-9
- By:
- Publication type:
- Article
Parental imprinting of an IGF-2 transgene.
- Published in:
- Molecular Reproduction & Development, 1993, v. 35, n. 4, p. 382, doi. 10.1002/mrd.1080350411
- By:
- Publication type:
- Article
Monochorionic twins discordant for mosaic trisomy 14.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 5, p. 1227, doi. 10.1002/ajmg.a.36407
- By:
- Publication type:
- Article
An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 787, doi. 10.1002/ajmg.a.35841
- By:
- Publication type:
- Article
TRISOMY 16 MOSAICISM IN AMNIOTIC FLUID CELL CULTURES.
- Published in:
- Prenatal Diagnosis, 1996, v. 16, n. 8, p. 749, doi. 10.1002/(SICI)1097-0223(199608)16:8<749::AID-PD935>3.0.CO;2-C
- By:
- Publication type:
- Article
An Integrated Human/Murine Transcriptome and Pathway Approach To Identify Prenatal Treatments For Down Syndrome.
- Published in:
- Scientific Reports, 2016, p. 32353, doi. 10.1038/srep32353
- By:
- Publication type:
- Article
Immunocytochemical Evidence for Methylation of the Inactive X Chromosome in Human Fetal Oogonia.
- Published in:
- Proceedings of the Society for Experimental Biology & Medicine, 1987, v. 186, n. 2, p. 223, doi. 10.3181/00379727-186-42606
- By:
- Publication type:
- Article
Transcriptomic analysis of cell-free fetal RNA suggests a specific molecular phenotype in trisomy 18.
- Published in:
- Human Genetics, 2011, v. 129, n. 3, p. 295, doi. 10.1007/s00439-010-0923-3
- By:
- Publication type:
- Article
Updated 2013 College of American Pathologists/American Society of Clinical Oncology (CAP/ASCO) guideline recommendations for human epidermal growth factor receptor 2 (HER2) fluorescent in situ hybridization (FISH) testing increase HER2 positive and HER2 equivocal breast cancer cases; retrospective study of HER2 FISH results of 836 invasive breast cancers
- Published in:
- Breast Cancer Research & Treatment, 2016, v. 157, n. 3, p. 405, doi. 10.1007/s10549-016-3824-x
- By:
- Publication type:
- Article
Applications of fluorescence spectroscopy to molecular cytogenetics.
- Published in:
- Biopolymers, 1985, v. 24, n. 1, p. 77, doi. 10.1002/bip.360240108
- By:
- Publication type:
- Article
Global Gene Expression Analysis of the Living Human Fetus Using Cell-Free Messenger RNA in Amniotic Fluid.
- Published in:
- JAMA: Journal of the American Medical Association, 2005, v. 293, n. 7, p. 836, doi. 10.1001/jama.293.7.836
- By:
- Publication type:
- Article
Attitudes Toward Cystic Fibrosis Carrier and Prenatal Testing and Utilization of Carrier Testing Among Relatives of Individuals with Cystic Fibrosis.
- Published in:
- Journal of Genetic Counseling, 1999, v. 8, n. 1, p. 17, doi. 10.1023/A:1022830519602
- By:
- Publication type:
- Article
Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Genetic and phenotypic diversity of NHE 6 mutations in Christianson syndrome.
- Published in:
- Annals of Neurology, 2014, v. 76, n. 4, p. 581, doi. 10.1002/ana.24225
- By:
- Publication type:
- Article
Xq;autosome translocation in POF: Xq27.2 deletion resulting in haploinsufficiency for SPANX.
- Published in:
- 2012
- By:
- Publication type:
- Report
Array-CGH analysis of cell-free fetal DNA in 10 mL of amniotic fluid supernatant.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Use of Y chromosome specific probes to detect low level sex chromosome mosaicism.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 5, p. 445, doi. 10.1111/j.1399-0004.1986.tb00519.x
- By:
- Publication type:
- Article
Homology of lubricin and superficial zone protein (SZP): Products of megakaryocyte stimulating factor (MSF) gene expression by human synovial fibroblasts and articular chondrocytes localized to chromosome 1q25.
- Published in:
- Journal of Orthopaedic Research, 2001, v. 19, n. 4, p. 677, doi. 10.1016/S0736-0266(00)00040-1
- By:
- Publication type:
- Article