Afifi HH - Search Results

1

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.

Abdel-Salam GMH, Sayed ISM, Afifi HH, Abdel-Ghafar SF, Abouzaid MR, Ismail SI, Aglan MS, Issa MY, El-Bassyouni HT, El-Kamah G, Effat LK, Eid M, Zaki MS, Temtamy SA, Abdel-Hamid MS. Abdel-Salam GMH, et al. Among authors: afifi hh. Am J Med Genet A. 2020 Jun;182(6):1407-1420. doi: 10.1002/ajmg.a.61585. Epub 2020 Apr 8. Am J Med Genet A. 2020. PMID: 32267100

2

An epidemiological/genetic study of mental subnormality in Assiut Governorate, Egypt.

Temtamy SA, Kandil MR, Demerdash AM, Hassan WA, Meguid NA, Afifi HH. Temtamy SA, et al. Among authors: afifi hh. Clin Genet. 1994 Nov;46(5):347-51. doi: 10.1111/j.1399-0004.1994.tb04176.x. Clin Genet. 1994. PMID: 7889643

3

COFS syndrome with familial 1;16 translocation.

Temtamy SA, Meguid NA, Mahmoud A, Afifi HH, Gerzawy A, Zaki MS. Temtamy SA, et al. Among authors: afifi hh. Clin Genet. 1996 Oct;50(4):240-3. doi: 10.1111/j.1399-0004.1996.tb02635.x. Clin Genet. 1996. PMID: 9001808

4

GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva.

Meguid NA, Afifi HH, Ramzy MI, Hindawy A, Temtamy SA. Meguid NA, et al. Among authors: afifi hh. Clin Genet. 1997 Aug;52(2):110-5. doi: 10.1111/j.1399-0004.1997.tb02527.x. Clin Genet. 1997. PMID: 9298746

5

Growth charts of Egyptian children with Down syndrome (0-36 months).

Meguid NA, El-Kotoury AI, Abdel-Salam GM, El-Ruby MO, Afifi HH. Meguid NA, et al. Among authors: afifi hh. East Mediterr Health J. 2004 Jan-Mar;10(1-2):106-15. East Mediterr Health J. 2004. PMID: 16201715 Free article.

6

Mandibuloacral dysplasia: a report of two Egyptian cases.

Afifi HH, El-Bassyouni HT. Afifi HH, et al. Genet Couns. 2005;16(4):353-62. Genet Couns. 2005. PMID: 16440877

7

Oto-spondylo-megaepiphyseal dysplasia (OSMED): clinical and radiological findings in sibs homozygous for premature stop codon mutation in the COL11A2 gene.

Temtamy SA, Männikkö M, Abdel-Salam GM, Hassan NA, Ala-Kokko L, Afifi HH. Temtamy SA, et al. Among authors: afifi hh. Am J Med Genet A. 2006 Jun 1;140(11):1189-95. doi: 10.1002/ajmg.a.31205. Am J Med Genet A. 2006. PMID: 16637051

8

Elejalde syndrome: clinical and histopathological findings in an Egyptian male.

Afifi HH, Zaki MS, El-Kamah GY, El-Darouti M. Afifi HH, et al. Genet Couns. 2007;18(2):179-88. Genet Couns. 2007. PMID: 17710870

9

Distal 11q monosomy syndrome: a report of two Egyptian sibs with normal parental karyotypes confirmed by molecular cytogenetics.

Afifi HH, Zaki MS, El-Gerzawy AM, Kayed HF. Afifi HH, et al. Genet Couns. 2008;19(1):47-58. Genet Couns. 2008. PMID: 18564501

10

Anorectal anomalies, diaphragmatic defect, cleft palate, lower lip pits, hypopigmentation and hypogammaglobulinemia A in Kabuki syndrome: a rare combination.

Abdel-Salam GM, Afifi HH, Eid MM, el-Badry TH, Kholoussi NM. Abdel-Salam GM, et al. Among authors: afifi hh. Genet Couns. 2008;19(3):309-17. Genet Couns. 2008. PMID: 18990987

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