نتایج جستجو برای: trisomy 9

تعداد نتایج: 487797  

Journal: :Cancer research 1992
M Thangavelu L Snyder J Anastasi M M Le Beau M Kirven G Picchio D E Mosier J D Rowley

We analyzed the karyotype of 27 B-cell lymphomas of human origin that developed in mice with severe combined immunodeficiency disease following the injection of peripheral blood leukocytes from Epstein-Barr virus-seropositive donors. Three tumors had clonal abnormalities detected with conventional techniques, 2 had trisomy 11, and 1 had a del(6)(q21q25). One other tumor had trisomy 11 detected ...

Journal: :Journal of medical genetics 1987
T Mattina G Sorge G Milone R Garozzo L Conti

A case of trisomy 9p syndrome is reported. The karyotype showed a tandem duplication of the short arm and of the inverted heterochromatic block of chromosome 9. Unequal sister chromatid exchange seems to be the only possible cause of this finding.

Journal: :مجله پزشکی مولکولی 0
najmeh ahangari department of genetics and biotechnology, faculty of medicine, hormozgan university of medical sciences, bandae abbas, iran mohammad doosti doosti department of molecular genetics, hope generation genetic polyclinic, mashhad, iran elaheh ahangari department od statistics, mashhad university of payam-e-noor, mashhad, iran. nafise baradarn rafiee department of obstetrics and gynecology, emam reza hospital, mashhad university of medical sciences, mashhad, iran ehsan ghayoor karimiani department of molecular genetics, honorary research associate, university of manchester, uk

introduction: the most common chromosomal abnormalities detected in perinatal period are aneuploidies of chromosome 21, 18, 13, x and y. the aim of this study is to assess referral reasons for invasive diagnostic method using rapid qf-pcr for fetal chromosomal abnormalities in gynecologists’ referrals. methods: a retrospective study of results was performed on data between september 2015 and ju...

Journal: :reports of biochemistry and molecular biology 0
aliakbar rahbarimanesh bahrami hospital, medical sciences/university of tehran, iran, po box 14155-1595 pupak derakhshandeh-peykar tel.: +49 89- 15254230228; fax: +49 89- 309088666 amirhassan barkhordari bahrami hospital, medical sciences/university of tehran, iran, po box 14155-1595 reza ebrahimzadeh-vesal department of medical genetics, medical sciences/university of tehran, iran, po box 14155-1595 soja shamizadeh kalkhoran bahrami hospital, medical sciences/university of tehran, iran, po box 14155-1595

background: here we describe a new case of partial distal 10q trisomy in a 6-year-old iranian girl from healthy parents with mental, growth, and psychomotor retardations. methods: additional clinical features include dysmorphic craniofacial features, microcephaly, bilateral hydronephrosis without heart problems, small and rotated low-set ears, bow-shaped mouth, abnormal teeth, short neck, and a...

Journal: :Pediatrics 2014
Nansi S Boghossian Nellie I Hansen Edward F Bell Barbara J Stoll Jeffrey C Murray John C Carey Ira Adams-Chapman Seetha Shankaran Michele C Walsh Abbot R Laptook Roger G Faix Nancy S Newman Ellen C Hale Abhik Das Leslie D Wilson Angelita M Hensman Cathy Grisby Monica V Collins Diana M Vasil Joanne Finkle Deanna Maffett M Bethany Ball Conra B Lacy Rebecca Bara Rosemary D Higgins

OBJECTIVE Little is known about how very low birth weight (VLBW) affects survival and morbidities among infants with trisomy 13 (T13) or trisomy 18 (T18). We examined the care plans for VLBW infants with T13 or T18 and compared their risks of mortality and neonatal morbidities with VLBW infants with trisomy 21 and VLBW infants without birth defects. METHODS Infants with birth weight 401 to 15...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1998
J C Byrd D Lawrence D C Arthur M J Pettenati R Tantravahi M Qumsiyeh J Stamberg F R Davey C A Schiffer C D Bloomfield

To date, neither the clinical significance of isolated trisomy 8, the most frequent trisomy in acute myeloid leukemia (AML), nor the effect of age within a single cytogenetic group has been examined. We report a large cohort of adult trisomy 8 patients and examine whether increasing age within a homogeneous cytogenetic group alters clinical outcome. Characteristics and outcome of patients with ...

Journal: :Frontiers in Medicine 2023

Objective Prenatal ultrasound features, associated anomalies and genetic abnormalities of microtia cases were analyzed to explore the feasibility value prenatal for diagnosis microtia. Methods The ultrasonographic anomalies, chromosome examination results follow-up 81 fetuses with congenital retrospectively. Results Among diagnosed after birth, 2 missed on ultrasound, 1 case was as unilateral b...

Journal: :Journal of medical genetics 1979
J M Cowen S Walker F Harris

A 9-year-old boy with classical clinical features of trisomy 13 (Patau's syndrome), with confirmation on chromosome analysis of blood and skin, is reported in view of his relative longevity.

Journal: :Proceedings of the Japan Academy, Series B 1980

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