| |
| Home - Health_Conditions - Opitz Syndrome | |
| Page 3 41-60 of 93 Back | 1 | 2 | 3 | 4 | 5 | Next 20 |
| 41. Entrez-PubMed opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a secondlocus on 22q11.2. Robin NH, Feldman GJ, Aronson AL, Mitchell HF, Weksberg R http://www.biomedcentral.com/pubmed/7493033 | |
|
| 42. Entrez-PubMed Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome. opitz syndromemaps to at least two loci, one on Xp, the other on 22q11.2. MeSH Terms http://www.biomedcentral.com/pubmed/8882786 | |
|
| 43. Smith, Lemli Et Opitz (syndrome De) Translate this page Smith, Lemli et Opitz (syndrome de). Voir également 13. En anglais Smith-Lemli-opitz syndrome. Synonyme syndrome RSH. Ensemble http://www.vulgaris-medical.com/texts/smitopit.html | |
|
| 44. Health Library - Opitz Syndrome opitz syndrome. International. Founded 1994.Support, encouragement, education, andsharing of successes and ideas for families affected by OpitzG/BBB Syndrome. http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29o |
| 45. Health Library - Opitz G/BBB Syndrome opitz syndrome. Disorder Subdivisions. General Discussion. Opitz G/BBB Syndromeor opitz syndrome is a genetic disorder that may be evident at birth. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw |
| 46. Health Library - Opitz Syndrome opitz syndrome. International. Founded 1994.Support, encouragement, education, andsharing of successes and ideas for families affected by OpitzG/BBB Syndrome. http://www.laurushealth.com/library/healthguide/selfhelp/topic.asp?hwid=shc29opi |
| 47. Health Library - Smith Lemli Opitz Syndrome Smith Lemli opitz syndrome. Synonyms Disorder Subdivisions General DiscussionResources SmithLemli-opitz syndrome is a hereditary developmental disorder. http://www.laurushealth.com/library/healthguide/illnessconditions/topic.asp?hwid |
| 48. Workshop On Smith-Lemli-Opitz Syndrome - Office Of Rare Diseases Workshop on SmithLemli-opitz syndrome co-sponsored by the Officeof Rare Diseases at NIH. National Institute of Child Health and http://rarediseases.info.nih.gov/news-reports/workshops/smith950926.html | |
|
| 49. BENCHMARK Analysis Of Smith-Lemli-Opitz Syndrome Translate this page BENCHMARK analysis of Smith-Lemli-opitz syndrome, G2D Home. GO TO The numberindicates the strength of association to Smith-Lemli-opitz syndrome. http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U6589 |
| 50. Opitz G/BBB Syndrome Support network for family members whose children have OpitzG/BBB syndrome.Category Health Conditions and Diseases opitz syndrome...... You have reached the website of of the Opitz G/BBB Family Network. For moreinformation on Opitz G/BBB syndrome and its challenges click to enter. http://www.rkymtnhi.com/opitz/ | |
|
| 51. References For Smith-Lemli-Opitz Syndrome With The MeSH Term References for SmithLemli-opitz syndrome with the MeSH term Smith-Lemli-OpitzSyndrome, G2D Home. PMID and date. Follow the link http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Smith-Lemli-Opitz_Sy |
| 52. Smith-lemli-opitz, Syndrome : Sites Et Documents Francophones Translate this page Smith-lemli-opitz, Syndrome. Arborescence(s) du thesaurus MeSH contenant lemot-clé Smith-Lemli-Opitz, syndrome Smith-Lemli-opitz syndrome http://www.chu-rouen.fr/ssf/pathol/smithlemliopitzsyndrome.html | |
|
| 53. 502 A Mouse Model For The Smith-Lemli-Opitz Syndrome (SLOS). Program Nr 502 A mouse model for the SmithLemli-opitz syndrome (SLOS).GS Tint 1,2 , H. Waage 3 , KK Sulik 3 , FF Moebius 4 , BU http://www.faseb.org/genetics/ashg99/f502.htm |
| 54. ClinicalTrials.gov - Linking Patients To Medical Research: Study Details Study of SmithLemli-opitz syndrome. Opitz JM. RSH/SLO ( Smith-Lemli-Opitz ) syndromehistorical, genetic, and developmental considerations. Am J Med Genet. http://www.clinicaltrials.gov/ct/gui/show/NCT00001721?order=6 |
| 55. ClinicalTrials.gov - Linking Patients To Medical Research: Study Details Estimation of the Carrier Frequency and Incidence of SmithLemli-OpitzSyndrome in African Americans. Condition. Smith-Lemli-opitz syndrome. http://www.clinicaltrials.gov/ct/gui/show/NCT00017732?order=34 |
| 56. Health Library - Smith Lemli Opitz Syndrome Smith Lemli opitz syndrome. Synonyms Disorder Subdivisions General DiscussionResources SmithLemli-opitz syndrome is a hereditary developmental disorder. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid= |
| 57. DHCR7 Translate this page Reference. CM004033, 1, ATGg-ATA, Met-Ile, Smith-Lemli-opitz syndrome,1. CM001121, 37, TGGt-TGA, Trp-Term, Smith-Lemli-opitz syndrome, 2. CM980542, http://www.uwcm.ac.uk/uwcm/mg/ns/1/9835302.html | |
|
| 58. Opitz Syndrome : Meddie Health Search (Rating 0.00 Votes 0) Rate It. National Library of Medicine OS Opitzsyndrome, the synonyms, a summary and a list of major features. http://www.meddie.com/search/Health/Conditions_and_Diseases/Genetic_Disorders/Op | |
|
| 59. Smith Lemli Opitz Syndrome : Meddie Health Search search options. Home Health Conditions and Diseases GeneticDisorders Smith Lemli opitz syndrome. ITEMS LINKS Emergency http://www.meddie.com/search/Health/Conditions_and_Diseases/Genetic_Disorders/Sm | |
|
| 60. LU:research - Lund University Institutional Archive Full text available as Title The opitz syndrome gene mid1 istranscribed from a human endogenous retroviral promoter. Authors http://eprints.lub.lu.se/archive/00011532/ | |
|
| Page 3 41-60 of 93 Back | 1 | 2 | 3 | 4 | 5 | Next 20 |
