- Home
- » Tags
- » Turner syndrome
Top View
- Turner's Syndrome in Males Pierre Caron
- Molecular Testing for Fragile X Syndrome: Lessons Learned from 119,232 Tests Performed in a Clinical Laboratory Charles M
- Reproductive and Obstetric Outcomes in Mosaic Turner's Syndrome
- Examination of Trisomy 13, 18 and 21 Foetal Tissues at Different Gestational Ages Using FISH
- Analysis of Genotype, Phenotype, and Age Progression in Phelan-Mcdermid Syndrome Sara Sarasua Clemson University, [email protected]
- Laboratory Guideline for Turner Syndrome Daynna J
- Syndrome Review 1: Autosomal Trisomies and Sex Chromosome
- Bleeding Disorders in Congenital Syndromes Susmita N
- CHROMOSOMAL ABNORMALITIES Chromosomal Abnormalities
- Allogeneic Stem Cell Transplantation from Donors with Mosaic Turner Syndrome
- Retrospective Karyotype Study in Mentally Retarded Patients
- Turner Syndrome
- A Mother with Variant Turner Syndrome and Two Daughters with Trisomy X: a Case Report
- Cognitive, Behavioral, and Neural Consequences of Sex Chromosome Aneuploidy
- Chromosomal Abnormalities and Atrial Fibrillation and Ischemic
- A Common Cause for Phelan-Mcdermid Syndrome and Neurofibromatosis Type 2: One Ring to Bind Them Ariel M
- Turner Syndrome and Its Variants Turner Sendromu Ve Varyantları
- Epigenetics in Turner Syndrome Francisco Álvarez-Nava1* and Roberto Lanes2
- NIH Research Plan on Fragile X Syndrome and Associated Disorders
- Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders
- Comorbidity Landscape of the Danish Patient Population Affected by Chromosome Abnormalities
- Triple X Syndrome Also Called Trisomy X
- Syndrome Toll-Free Information and Support Helpline
- NIPT: High Risk for Sex Chromosome Disorder
- Aneuploidy – What Are the Outcomes ?
- Fact Sheet 40| TURNER SYNDROME This Fact Sheet Describes The
- The Human Genome
- Woman with Turner Syndrome and Her Child with Acute Leukemia (A Case Report) N
- Molecular Biology of Turner's Syndrome Arch Dis Child: First Published As 10.1136/Adc.72.4.285 on 1 April 1995
- Tetrasomy 15Q26: a Distinct Syndrome Or Shprintzen-Goldberg Syndrome Phenocopy?
- Turner Syndrome: Addressing How Misconceptions Overshadow Opportunities for a “Normal” Life
- Is It Time to Start Newbornscreening Forturner Syndrome? JSM Genet Genomics 4(1): 1023
- Two Rare Variants of Down Syndrome: Down-Turner Syndrome and Down Syndrome with Translocation (13;14): a Case Report
- An Isodicentric X Chromosome with Short Arm Fusion in a Woman Without
- Double Aneuploidy 48,ХХХ,+21 of a Bulgarian Newborn with Down
- Psychfeaturesinchildren.Pdf
- Patient-Derived Induced Pluripotent Stem Cells (Ipscs)
- Apropos of Three Cases of Sex Chromosome Anomalies
- Turner Syndrome
- Fragile X Syndrome
- Fragile X Syndrome Full Mutation Females at Increased Risk for Mosaic Turner Syndrome: Fragile X Leads to Chromosome Loss
- A Case Report of Spontaneous Pregnancy in a Mosaic Turner
- Cytogenetic and Genomic Analysis of a Patient with Turner Syndrome and T(2;12): a Case Report Paola E
- Common and Specific Impairments in Attention Functioning in Girls with Chromosome 22Q11.2 Deletion, Fragile X Or Turner Syndromes
- Down-Turner Syndrome: Case Report and Review J Med Genet: First Published As 10.1136/Jmg.31.10.807 on 1 October 1994
- A Review of Trisomy X (47,XXX) Orphanet Pseudoautosomal Region
- Turner Syndrome Caused by Rare Complex Structural Abnormalities Involving Chromosome X
- Cognitive and Neurological Aspects of Sex Chromosome Aneuploidies
- Dysgerminoma with a Somatic Exon 17 KIT Mutation and SHH Pathway Activation in a Girl with Turner Syndrome
- Chromosome Abnormalities Reference
- Chromosome Analysisanalysis Nationalnational DNADNA Dayday Aprilapril 25,25, 20052005
- A 14 YEAR-OLD GIRL with TURNER SYNDROME of COMPLICATED KARYOTYPE; 45,X/47,XY, + 18,-- 19, +Der(19),T(Y;19) (Q12 ;Pl 3.3)
- Sex Chromosome Aneuploidies