Wolf–Hirschhorn syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Wolf–Hirschhorn syndrome" in English language version.

refsWebsite

Global rank English rank

8nih.gov

4^th place

6doi.org

2^nd place

2semanticscholar.org

11^th place

8^th place

2medlineplus.gov

1,581^st place

1,299^th place

1omim.org

4,380^th place

4,305^th place

1web.archive.org

1^st place

1orpha.net

3,537^th place

7,177^th place

1rarediseases.org

5,181^st place

3,260^th place

1clevelandclinic.org

4,925^th place

3,597^th place

clevelandclinic.org

my.clevelandclinic.org

"Wolf-Hirschhorn Syndrome: Symptoms & Causes". Cleveland Clinic. Retrieved 2023-10-10.

doi.org

Dufke A, Seidel J, Schöning M, Döbler-Neumann M, Kelbova C, Liehr T, Beensen V, Backsch C, Klein-Vogler U, Enders H (2000). "Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome". Cytogenetics and Cell Genetics. 91 (1–4): 81–4. doi:10.1159/000056823. PMID 11173835. S2CID 19641395.
Paradowska-Stolarz AM (2014). "Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome". Adv Clin Exp Med. 23 (3): 485–9. doi:10.17219/acem/24111. PMID 24979523.
Hanley-Lopez J, Estabrooks LL, Stiehm R (July 1998). "Antibody deficiency in Wolf-Hirschhorn syndrome". The Journal of Pediatrics. 133 (1): 141–3. doi:10.1016/S0022-3476(98)70194-5. PMID 9672528.
Rauch A, Schellmoser S, Kraus C, Dörr HG, Trautmann U, Altherr MR, Pfeiffer RA, Reis A (April 2001). "First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation". American Journal of Medical Genetics. 99 (4): 338–42. doi:10.1002/ajmg.1203. PMID 11252005.
Mbuyi-Musanzayi, Sébastien; Lumaka, Aimé; Kasole, Toni; Ilunga, Erick; Asani, Bienvenu; Tshilobo, Prosper; Muenze, Prosper; Reychler, Hervé; Katombe, François; Devriendt, Koenraad (September 2017). "Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa". Journal of Pediatric Genetics. 06 (3): 186–190. doi:10.1055/s-0037-1599194. PMC 5548528. PMID 28794913.
Hirschhorn K, Cooper HL, Firschein IL (1961). "Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion". Humangenetik. 1 (5): 479–82. doi:10.1007/bf00279124. PMID 5895684. S2CID 32805973.

medlineplus.gov

"Wolf-Hirschhorn syndrome: MedlinePlus Genetics". medlineplus.gov. Retrieved 2023-10-10.
"Wolf-Hirschhorn syndrome: MedlinePlus Genetics". medlineplus.gov. Retrieved 2023-10-10.

nih.gov

pubmed.ncbi.nlm.nih.gov

Dufke A, Seidel J, Schöning M, Döbler-Neumann M, Kelbova C, Liehr T, Beensen V, Backsch C, Klein-Vogler U, Enders H (2000). "Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome". Cytogenetics and Cell Genetics. 91 (1–4): 81–4. doi:10.1159/000056823. PMID 11173835. S2CID 19641395.
Paradowska-Stolarz AM (2014). "Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome". Adv Clin Exp Med. 23 (3): 485–9. doi:10.17219/acem/24111. PMID 24979523.
Hanley-Lopez J, Estabrooks LL, Stiehm R (July 1998). "Antibody deficiency in Wolf-Hirschhorn syndrome". The Journal of Pediatrics. 133 (1): 141–3. doi:10.1016/S0022-3476(98)70194-5. PMID 9672528.
Rauch A, Schellmoser S, Kraus C, Dörr HG, Trautmann U, Altherr MR, Pfeiffer RA, Reis A (April 2001). "First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation". American Journal of Medical Genetics. 99 (4): 338–42. doi:10.1002/ajmg.1203. PMID 11252005.
Mbuyi-Musanzayi, Sébastien; Lumaka, Aimé; Kasole, Toni; Ilunga, Erick; Asani, Bienvenu; Tshilobo, Prosper; Muenze, Prosper; Reychler, Hervé; Katombe, François; Devriendt, Koenraad (September 2017). "Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa". Journal of Pediatric Genetics. 06 (3): 186–190. doi:10.1055/s-0037-1599194. PMC 5548528. PMID 28794913.
Hirschhorn K, Cooper HL, Firschein IL (1961). "Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion". Humangenetik. 1 (5): 479–82. doi:10.1007/bf00279124. PMID 5895684. S2CID 32805973.
Wolf U, Reinwein H, Porsch R, Schröter R, Baitsch H (1965). "[Deficiency on the short arms of a chromosome No. 4]". Humangenetik (in German). 1 (5): 397–413. PMID 5868696.

ncbi.nlm.nih.gov

Mbuyi-Musanzayi, Sébastien; Lumaka, Aimé; Kasole, Toni; Ilunga, Erick; Asani, Bienvenu; Tshilobo, Prosper; Muenze, Prosper; Reychler, Hervé; Katombe, François; Devriendt, Koenraad (September 2017). "Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa". Journal of Pediatric Genetics. 06 (3): 186–190. doi:10.1055/s-0037-1599194. PMC 5548528. PMID 28794913.

omim.org

Online Mendelian Inheritance in Man (OMIM): Wolf-Hirschhorn syndrome - 194190

orpha.net

Wieczorek D (September 2003). "Wolf-Hirschhorn syndrome" (PDF). Orphanet encyclopedia. Archived from the original (PDF) on 2021-03-09. Retrieved 2004-11-13.

rarediseases.org

"Wolf-Hirschhorn Syndrome - Symptoms, Causes, Treatment | NORD". rarediseases.org. Retrieved 2023-10-10.

semanticscholar.org

api.semanticscholar.org

Dufke A, Seidel J, Schöning M, Döbler-Neumann M, Kelbova C, Liehr T, Beensen V, Backsch C, Klein-Vogler U, Enders H (2000). "Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome". Cytogenetics and Cell Genetics. 91 (1–4): 81–4. doi:10.1159/000056823. PMID 11173835. S2CID 19641395.
Hirschhorn K, Cooper HL, Firschein IL (1961). "Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion". Humangenetik. 1 (5): 479–82. doi:10.1007/bf00279124. PMID 5895684. S2CID 32805973.

web.archive.org

Wieczorek D (September 2003). "Wolf-Hirschhorn syndrome" (PDF). Orphanet encyclopedia. Archived from the original (PDF) on 2021-03-09. Retrieved 2004-11-13.