1
0
0
News
Netzwerk-Profile
LinkedIn: Genet A. | LinkedIn
Genet A.s berufliches Profil anzeigen LinkedIn ist das weltweit größte professionelle Netzwerk, das Fach- und Führungskräften wie Genet A. dabei hilft, interne ...
LinkedIn: Genet A. – Auszubildende – Universitätsklinikum Würzburglinkedin.com
Sehen Sie sich das Profil von Genet A. im größten Business-Netzwerk der Welt an. Im Profil von Genet A. ist 1 Job angegeben. Auf LinkedIn können Sie sich ...
LinkedIn: Genet A. - Engineering lecturer - Kirklees College | LinkedInuk.linkedin.com › genet-a-81a81819b
View Genet A.'s profile on LinkedIn, the world's largest professional community. Genet has 1 job listed on their profile. See the complete profile on ...
LinkedIn: Genet A. Gebru | Berufsprofil - LinkedIn
größten beruflichen Netzwerk. Genet A. Gebru hat 6 Jobs im Profil angegeben.
Business-Profile
Genet A. from Ethiopia, 13 years of experience in Gender, ...DevelopmentAid
www.developmentaid.org
Genet A. is an expert in Gender, Monitoring & Evaluation, Training sectors with 13 years of experience from Ethiopia with Masters degree, speaks Amharic, ... Genet A. is an expert in Gender, Monitoring & Evaluation, Training sectors with 13 years of experience from Ethiopia with Masters degree, speaks Amharic, ...
Private Homepages
Down Syndrome | Birth DefectsCenters for Disease Control and Prevention (.gov)
www.cdc.gov
— Am J Med Genet A Jul;149A(7): Sherman SL, Allen EG, Bean LH, Freeman SB. Epidemiology of Down syndrome. Ment Retard Dev — Am J Med Genet A Jul;149A(7): Sherman SL, Allen EG, Bean LH, Freeman SB. Epidemiology of Down syndrome. Ment Retard Dev ...
Ausbildung
Brynn Levy, MSc, PhD | Pathology
www.pathology.columbia.edu
Am J Med Genet A Sep;161(9): Forman EJ, Hong KH, Ferry KM, Tao X, Taylor D, Levy B, Treff NR, Scott, Jr. RT. In vitro fertilization with single ...
Bücher
Pediatric Otolaryngology - Seite Google Books-Ergebnisseitegoogle.de
books.google.de
... Genet A ; 143A : Lezirovitz K , Pardono E , de Mello Auricchio MT , et al . Unexpected genetic heterogeneity in a large consanguineous ...
Primer on the Metabolic Bone Diseases and Disorders of ...google.de
books.google.de
... Genet A ;167A(12):2869– Krakow D, Rimoin DL. The skeletal dysplasias. Genet Med ;12(6):327– Provot S, Schipani E. Molecular mechanisms ...
Williams Textbook of Endocrinology E-Bookgoogle.de
books.google.de
... Genet A ;143a(9):973– Graham JM Jr, Lee J. Bosma arhinia microphthalmia syndrome. Am J Med Genet A ;140(2):189– Johnson VP ...
The Eye in Pediatric Systemic Disease - Google Books
books.google.co.uk
This book is the first of its kind to describe ocular manifestations of systemic diseases in the pediatric population. Written and edited by experts in areas...
Wissenschaftliche Veröffentlichungen
AG Skeletterkrankungen und genetische SyndromeUniklinik Köln
humangenetik.uk-koeln.de
A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q microdeletion syndrome. Am J Med Genet A ;173(8): A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q microdeletion syndrome. Am J Med Genet A ;173(8):
Atypical case of Wolfram syndrome revealed through targeted exome...
bmcmedgenet.biomedcentral.com
Am J Med Genet A , 143A (14): impairment. Am J Med Genet A , 155A (6): Am J Med Genet A , 125A (3):
Molekulare Endokrinologie — Deutsch
www.uniklinikum-dresden.de
Am J Med Genet A ;158A: Hackmann K, Matko S, Gerlach EM, von der Hagen M, Klink B, Schrock E, Rump A, Di Donato N. Partial deletion of ...
A deletion and a duplication in distal 22q11.2 deletion syndrome...
bmcmedgenet.biomedcentral.com
Individuals affected with DiGeorge and Velocardiofacial syndromes present with both phenotypic diversity and variable expressivity. The most frequent clinical...
Artikel & Meinungen
Meta-analysis and multidisciplinary consensus statement: exome...
www.nature.com
Marked yield of re-evaluating phenotype and exome/target sequencing data in 33 individuals with intellectual disabilities. Am J Med Genet A.
Sonstiges
Genet A. PallyBoyd & Jenerette
www.boydjen.com
Genet A. Pally - Associate. Genet A. Pally. Associate. Direct: ; ; · Download vCard. Areas Of Practice. Genet A. Pally - Associate. Genet A. Pally. Associate. Direct: ; ; · Download vCard. Areas Of Practice.
Nutritional phases in Prader-Willi syndromeNational Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von JL Miller · · Zitiert von: 461 — Am J Med Genet A May;155A(5): doi: ajmg.a Epub Apr 4. Authors. Jennifer L Miller , Christy H Lynn, Danielle C Driscoll ... von JL Miller · · Zitiert von: 461 — Am J Med Genet A May;155A(5): doi: ajmg.a Epub Apr 4. Authors. Jennifer L Miller , Christy H Lynn, Danielle C Driscoll ...
AM J MED GENET A | UKE Research PortalUKE
fis.uke.de
AM J MED GENET A - American journal of medical genetics. Part A ... & De Sandre-Giovannoli, A.In: AM J MED GENET A. 191, 9, p p ... AM J MED GENET A - American journal of medical genetics. Part A ... & De Sandre-Giovannoli, A.In: AM J MED GENET A. 191, 9, p p ...
The burden of rare diseasesNational Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von CR Ferreira · · Zitiert von: 366 — Am J Med Genet A Jun;179(6): doi: ajmg.a Epub Mar 18. Author. Carlos R Ferreira. Affiliation. 1 National Human Genome ... von CR Ferreira · · Zitiert von: 366 — Am J Med Genet A Jun;179(6): doi: ajmg.a Epub Mar 18. Author. Carlos R Ferreira. Affiliation. 1 National Human Genome ...
Journal - Am J Med Genet ANational Genomics Data Center
ngdc.cncb.ac.cn
Journal Abbr. Am J Med Genet A. Web of Sciences Category. Genetics & Heredity. Print ISSN, E-ISSN, NLM Catelog ID, -. Scopus Source ID ... Journal Abbr. Am J Med Genet A. Web of Sciences Category. Genetics & Heredity. Print ISSN, E-ISSN, NLM Catelog ID, -. Scopus Source ID ...
PIK3CA-related overgrowth spectrum (PROS) - PubMedNational Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von KM Keppler-Noreuil · · Zitiert von: 517 — PIK3CA-related overgrowth spectrum (PROS): diagnostic and testing eligibility criteria, differential diagnosis, and evaluation. Am J Med Genet A Feb;167A( ... von KM Keppler-Noreuil · · Zitiert von: 517 — PIK3CA-related overgrowth spectrum (PROS): diagnostic and testing eligibility criteria, differential diagnosis, and evaluation. Am J Med Genet A Feb;167A( ...
Genet A. Gebru - Human Resources Business Partner - Facebook ...
www.linkedin.com
größten beruflichen Netzwerk. 7 Jobs sind im Profil von Genet A. Gebru
aufgelistet.
GENET A. - Boston, Massachusetts, United Stateslinkedin.com
www.linkedin.com
View GENET A.'s profile on LinkedIn, the world's largest professional community. GENET's education is listed on their profile. See the complete profile on ...
Genet A. Pally PA - Attorneylinkedin.com
www.linkedin.com
Genet Pally. Attorney at Genet A. Pally PA. Genet A. Pally PA. Cape Coral Metropolitan Area. See your mutual connections. View mutual connections with Genet.
Genet A. | LinkedIn
www.linkedin.com
View Genet A.'s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Genet A. discover inside ...
Genet A. - Deputy Chief of Party \POTENTIAL Program ...
www.linkedin.com
View Genet A.'s profile on LinkedIn, the world's largest professional community. Genet has 5 jobs listed on their profile. See the complete profile on LinkedIn and ...
Genet A. Ebrahim - Impact and Development Fellow - S.O.U.L. ...
www.linkedin.com
View Genet A. Ebrahim's profile on LinkedIn, the world's largest professional community. Genet A. has 5 jobs listed on their profile. See the complete profile on ...
Genet A. Gebru - Human Resources Business Partner ...
www.linkedin.com
View Genet A. Gebru's profile on LinkedIn, the world's largest professional community. Genet A. has 6 jobs listed on their profile. See the complete profile on ...
Am J Med Genet A.: co-auth.: A.Reymond, I.Xenarios
www.genomyx.ch
Am J Med Genet A Mar 21. doi: ajmg.a [Epub ahead of print] Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome....
Agenesis of the Corpus Callosum ACC congenital disorder. Patient |...
patient.info
eCollection Schell-Apacik CC, Wagner K, Bihler M, et al; Agenesis and dysgenesis of the corpus callosum: clinical, genetic and Am J Med Genet A
AM J MED GENET A | UKE Research Portal
fis-uke.de
Kakar, N., Horn, D., Decker, E., Sowada, N., Kubisch, C., Ahmad, J., Borck, G. & Bergmann, C.In : AM J MED GENET A. 176, 2, p p.
J Genet Med
www.e-kjgm.org
Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11. Am J Med Genet A. 170, ...
Array Publications - Baylor Genetics
www.baylorgenetics.com
Am J Med Genet A Aug 15;137(1): PubMed PMID: ; Lennon PA, Cooper ML, Curtis MA, Lim C, Ou Z, Patel A, Cheung SW, Bacino CA.
Interstitial deletion of 14q24.3-q32.2 in a male patient with...
pubmed.ncbi.nlm.nih.gov
Distal interstitial deletions of chromosome 14 involving the 14q24-q23.2 region are rare, and only been reported so far in 20 patients. Ten of these patients...
Costello Syndrome - NORD (National Organization for Rare Disorders)
rarediseases.org
Am J Med Genet A ;146A(9): Kerr B, Allanson J, Delrue MA, Gripp KW, Lacombe D, Lin AE, Rauen KA. The diagnosis of Costello syndrome: ...
Verwandte Suchanfragen zu Genet A.
|
Personen Vorname "Genet" (65) Name |
sortiert nach Relevanz / Datum