Afifi HH - Search Results

1

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.

Mohamed AM, Kamel AK, Eid MM, Eid OM, Mekkawy M, Hussein SH, Zaki MS, Esmail S, Afifi HH, El-Kamah GY, Otaify GA, El-Awady HA, Elaidy A, Essa MY, El-Ruby M, Ashaat EA, Hammad SA, Mazen I, Abdel-Salam GMH, Aglan M, Temtamy S. Mohamed AM, et al. Among authors: afifi hh. Mol Genet Genomic Med. 2021 Nov;9(11):e1829. doi: 10.1002/mgg3.1829. Epub 2021 Oct 5. Mol Genet Genomic Med. 2021. PMID: 34609792 Free PMC article.

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

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

7

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

8

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

9

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

10

Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorder.

Zaki MS, Afifi HH, Barkovich AJ, Gleeson JG. Zaki MS, et al. Among authors: afifi hh. Am J Med Genet A. 2009 Aug;149A(8):1789-94. doi: 10.1002/ajmg.a.32983. Am J Med Genet A. 2009. PMID: 19610102 Free PMC article.

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