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12 Possible Causes for &, (Milne Edwards, 1857), Goniastrea, Haime,, australensis

Did you mean: &, (Milne, Edwards, 1857), Goniastrea, Haime, australensis

  • Vibrio

    Ampe, F. Barloy-Hubler, M. J. Barnett, A. Becker, P. Boistard, G. Bothe, M. Boutry, L. Bowser, J. Buhrmester, E. Cadieu, D. Capela, P. Chain, A. Cowie, R. W. Davis, S.[doi.org] Danovaro , Bacteria associated with the rapid tissue necrosis of stony corals , Environmental Microbiology , 9 , 7 , (1851-1857) , (2007) . Tom Defoirdt, Carol M.[doi.org] ., 2011 Species Vibrio coralliilyticus Ben-Haim et al., 2003 Species Vibrio crassostreae Faury et al., 2004 Species Vibrio cyclitrophicus Hedlund and Staley, 2001 Species[itis.gov] Sawabe, Fujimura, Niwa & Aono, 2007 Species Vibrio communis Chimetto, Cleenwerck, Alves, Silva, Brocchi, Willems, De Vos & Thompson, 2011 Species Vibrio coralliilyticus Ben-Haim[marinespecies.org] Ben-Haim. 2002 . Microbial diseases of corals and global warming. Environ. Microbiol. 4 : 318 -326. Ruimy, R., V. Breittmayer, P. Elbaze, B. Lafay, O. Boussemart, M.[doi.org] Edwards) , Aquaculture Research , 45 , 12 , (1989-1999) , (2013) .[doi.org]

    Missing: Goniastrea australensis
  • Three M Syndrome

    The existence of discrete inheritable units was first suggested by Gregor Mendel, from 1857 to 1864, in Brno, he studied inheritance patterns in 8000 common edible pea plants[wikivisually.com] Carnitin-Palmitoyl-Transferase II-Mangel CREBBP del Rubinstein-Taybi CSX ( NKX2-5) Atrial Septum Defect (ASD) (Vorhofseptumdefekt) CTNS Cystinose, nephropathisch CTSC del Papillon-Lefèvre, Haim-Munk[yumpu.com] 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY Syndrome Klinefelter Syndrome 50 Sutton Disease 40 XYY Syndrome 51 Sweet Syndrome 41[books.google.com] […] somatic IDH1 Glucocorticoid Defizienz MRAP, MC2R, NNT Glucocorticoid Defizienz ACTH Nonresponsiveness MC2R GLUT1 deficiency syndrome 2 SLC2A1 Gorlin-Goltz-Syndrom PTCH1 Haim-Munk-Syndrom[meduniwien.ac.at] 18 syndrome ( 1 Files ) Disease name: Trisomy 18 ICD 10: Q91.1 Synonyms : Edwards syndrome; trisomy E syndrome; chromosome 18, trisomy 18 complete; complete trisomy 18 syndrome[orphananesthesia.eu] Pityriasis Rubra Pilaris 34 Chromosome 9 Trisomy Mosaic 45 Pseudoxanthoma Elasticum 35 Pentasomy X 46 Pyoderma Gangrenosum 36 Trisomy 13 Syndrome 47 RothmundThomson Syndrome 37 Trisomy[books.google.com]

    Missing: Goniastrea australensis
  • Periventricular Leukomalacia

    Call us toll-free at (888) 592-1857 or complete this online contact form for a free evaluation of your child’s cerebral palsy case.[michigancerebralpalsyattorneys.com] Laura Toso, Sarah Poggi, Jane Park, Haim Einat, Robin Roberson, Veronica Dunlap, Jade Woodard, Daniel Abebe and Catherine Y.[doi.org] At prenatal US these cysts can be predictive of trisomy 18.[radiologyassistant.nl] Call Michigan Cerebral Palsy Attorneys at (888) 592-1857 or fill out this contact form online to learn if you have a case. Contact Our Team Sources “Brain Atlas.”[michigancerebralpalsyattorneys.com] About half of babies with Trisomy 18 show a CPC on ultrasound, but nearly all of these babies will also have other abnormalities on the ultrasound, especially in the heart[radiologyassistant.nl]

    Missing: Goniastrea australensis
  • Down Syndrome

    A total RNA 100 ng were labeled using LowInputQuick Amp Labeling kit (Agilent 5190–2305) following manufacturer instructions.[dx.doi.org] […] support”: attitudes toward disability rights and prenatal diagnosis among leaders of support groups for genetic disorders in Israel , Social Science & Medicine , 59 , 9 , (1857[doi.org] Spence and Haim Arie Abenhaim , The effect of assisted reproductive technology on the incidence of birth defects among livebirths , Archives of Gynecology and Obstetrics ,[doi.org] The positive predictive values for cfDNA testing versus standard screening were 45.5% versus 4.2% for trisomy 21 and 40.0% versus 8.3% for trisomy 18.[ncbi.nlm.nih.gov] In the primary analysis population of 1914 patients, the outcome was determined on the basis of the newborn physical examination in 1857 patients (97.0%) and on the basis[dx.doi.org] The results of the blood test, the nuchal translucency measurement and the mother's age are used to estimate the risk for Down syndrome and trisomy 18.[ucsfhealth.org]

    Missing: Goniastrea australensis
  • 14q11-q22 Microdeletion Syndrome

    Amp(1q23.3), amp(5q31.3), and del(12p13.31) retained independent prognostic value in multivariate analysis.[mdpi.com] Am J Med Genet A 2007;143:1850-1857 Shapira SK, McCaskill C, Northrup H, Spikes AS, Elder FF, et al: Chromosome 1p36 deletions: the clinical phenotype and molecular characterization[karger.com] […] keratoderma Guttmacher syndrome Gyrate atrophy of choroid and retina H syndrome H-ABC Haddad syndrome HADH deficiency HAE 2 HAE 3 HAE-I HAE-II HAE-III Hailey-Hailey disease Haim-Munk[csbg.cnb.csic.es] Probe Target Abnormality RB1 Trisomy 13 D18Z1 Trisomy 18 D21S259 Trisomy 21 DXZ1 Sex Chromosome Aneuploidy DYZ3 Sex Chromosome Aneuploidy Preliminary results are available[diagnosticcytogenetics.com] However there is limited and mixed information about the characteristics of epilepsy related to trisomy 18. Thus a common seizure phenotype has not...[infona.pl] ., were positive for the “triple trisomies” ( 18 , 19 )].[pnas.org]

    Missing: Goniastrea australensis
  • Strudwick Syndrome

    […] proteinphosphatase 1, regulatoriske subungfdit 12A PTPN11: proteintyrosinphosphatase, ikke-receptor typen 11 KRAS: V-Ki-ras2 Kirsten rotte sarkom viral onkogen homolog Sygdomme & amp[deersted.com] The existence of discrete inheritable units was first suggested by Gregor Mendel, from 1857 to 1864, in Brno, he studied inheritance patterns in 8000 common edible pea plants[wikivisually.com] Gynecomastia (familial, due to increased aromatase activity); Gyrate atrophy of choroid and retina with ornithinemia (B6 responsive or unresponsive); Hailey-Hailey disease; Haim-Munk[lens.org] […] trisomi 13 syndrom se trisomi 13 komplet trisomi 18 syndrom se trisomi 18 medfdt arvelig hmaturi se Alport syndrom medfdt progressive okulo-acoustico-cerebral degeneration[sundhed.cc] It uses “cranial electrotherapy stimulation” – 50-100 microamps of electricity (a microamp is a millionth of an amp) – to increase alpha brain waves.[telegraph.co.uk] Package Operating Temperature -40 C to 100 C Remote On/Off Very High Efficiency up to 97% Output Voltage Trim Tape & Reel Package Available 3 Year Warranty More Info TR10 1 Amp[xppower.com]

    Missing: Goniastrea australensis
  • Autosomal Dominant Benign Spinal Muscular Atrophy

    2 104310 (DAT; APOE E2/E3/E4-Allele 107741 ) Alzheimer-Demenz (familiär) Typ 3 607822 (DAT; PSEN1 104311 ) Alzheimer-Demenz (familiär) Typ 4 606889 (DAT; PSEN2 600759 ) AMP-Desaminase-Mangel[medizinische-genetik-dresden.de] The existence of discrete inheritable units was first suggested by Gregor Mendel, from 1857 to 1864, in Brno, he studied inheritance patterns in 8000 common edible pea plants[wikivisually.com] […] somatic IDH1 Glucocorticoid Defizienz MRAP, MC2R, NNT Glucocorticoid Defizienz ACTH Nonresponsiveness MC2R GLUT1 deficiency syndrome 2 SLC2A1 Gorlin-Goltz-Syndrom PTCH1 Haim-Munk-Syndrom[meduniwien.ac.at] 18 complete; complete trisomy 18 syndrome Emery-Dreifuss-Muskeldystrophie ( 2 Files ) Erkrankung: Emery-Dreifuss Muscular Dystrophy (EDMD) ICD 10: G71.0 Synonyme: Benign[orphananesthesia.eu] Archiv fur Psychiatrie und Nervenkrank, 1891; 22: 437–80] and (Johann) Hoffman [(1857–1919); ‘Ueber chronische spinale Muskelatrophie im Kindesalter auf familiärer Basis’.[academic.oup.com] […] dermatomyositis (onset 18 yrs) Edwards-Syndrom ( 1 Files ) Name der Erkrankung: Edwards-Syndrom ICD 10: Q91.1 Synonyme : Edwards syndrome; trisomy E syndrome; chromosome 18, trisomy[orphananesthesia.eu]

    Missing: Goniastrea australensis
  • Oculootoradial Syndrome

    […] sequencing study rh thelancet com and gr lrg more images on door syndrome omim Visualizations sc 1 th 199 Visualizations sc th also dataset omim gene disease associations rh amp[pezcame.com] […] of people with Tourette's. [3] The condition was named by Jean-Martin Charcot (1825–1893) on behalf of his resident, Georges Albert Édouard Brutus Gilles de la Tourette (1857[en.wikipedia.org] […] keratoderma Guttmacher syndrome Gyrate atrophy of choroid and retina H syndrome H-ABC Haddad syndrome HADH deficiency HAE 2 HAE 3 HAE-I HAE-II HAE-III Hailey-Hailey disease Haim-Munk[csbg.cnb.csic.es] Should exclude trisomy 18 by performing a karyotype. Delivery is recommended at a tertiary center to permit consultation with genetics, radiology, and orthopedics.[mhmedical.com] 18Trisomie 18 en mosaique •Trisomie 18p •Trisomie 18q •Trisomie 19q •Trisomie 1 en mosaique •Trisomie 1p21 p32 •Trisomie 1q12 q21 •Trisomie 1q32 qter •Trisomie 1q42 11[reconexion.es.tl] Aminoaciduria, Hartnup type Amish infantile epilepsy syndrome Amish lethal microcephaly Amish nemaline myopathy AML AML with CEBPA somatic mutations AMME complex AMME syndrome AMP[csbg.cnb.csic.es]

    Missing: Goniastrea australensis
  • Amaurosis-Hypertrichosis Syndrome

    Mutations in the genes encoding the cyclic-AMP regulated enhanced binding protein (CREBBP) and the E1A binding protein p300 (EP300) have been found in patients with this syndrome[link.springer.com] Russian dermatologist Nikolai Mansurov took this photograph of a patient with Ambras syndrome, circa 1857.[blogs.plos.org] Hepatocellular carcinoma) CTNND2 (Mental retardation in cri-du-chat syndrome) CTNS (Cystinosis, late-onset juvenile or adolescent nephropathic) CTSA (Galactosialidosis) CTSC (Haim-Munk[en.praenatal-medizin.de] 18 Edwards: Eye Findings Ankyloblepharon Connection between the upper and lower lids Trisomy 21 Downs Syndrome: Eye Findings Keratoconus: common (7 times population risk)[quizlet.com] […] arcuate eyelashes - Nystagmus - High Myopia Smith Magenis: Genetics and Eye Findings - 17p11 - Iris anomalies (70%) - Microcornea (50%) - Myopia (42%) - Strabismus (32%) Trisomy[quizlet.com]

    Missing: Goniastrea australensis
  • Severe Infantile Carnitine Palmitoyl Transferase II Deficiency

    Genetic Testing - Adenosine monophosphate deaminase -AMP-, ... deficiency; Myoadenylate deaminase deficiency (Adenosine monophosphate deaminase deficiency -AMP-; myoadenylate[ivami.com] Chapter 83:1857-1895.[genico.ch] Retardation due to IGF1R Gyrate Atrophy Gyrate Atrophy with Pyridoxine-responsive Ornithinemia Haemoglobin H Disease Haemorrhagic Telangiectasia 1 Hailey-Hailey Disease Haim-Munk[sequencing.com] Regulation of cyclic AMP by extracellular ATP in cultured brain capillary endothelial cells.[journals.plos.org] Genetic Testing - Trisomy 18 (Trisomy 18) - Chromosome 18.[ivami.com] Chapter 83, pg. 1857 - 1895.[genico.ch]

    Missing: Goniastrea australensis