PubMed (OMIM) for id: 10617

Year	Number of Results
1950	1
1952	1
1959	1
1962	2
1965	1
1968	1
1975	1
1977	1
1981	1
1982	1
1987	1
1988	2
1990	1
1991	1
1994	2
1996	2
2000	1
2002	1
2003	4
2024	0

1

The Pelger-anomaly in man and rabbit; a mendelian character of the nuclei of the leucocytes.

NACHTSHEIM H. NACHTSHEIM H. J Hered. 1950 May;41(5):131-7. doi: 10.1093/oxfordjournals.jhered.a106108. J Hered. 1950. PMID: 15436969 No abstract available.

2

Homozygous form of Pelger-Huët's nuclear anomaly in man.

HAVERKAMP BEGEMANN N, VAN LOOKEREN CAMPAGNE A. HAVERKAMP BEGEMANN N, et al. Acta Haematol. 1952 May;7(5):295-303. doi: 10.1159/000204063. Acta Haematol. 1952. PMID: 14932764 No abstract available.

3

Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes.

Oosterwijk JC, Mansour S, van Noort G, Waterham HR, Hall CM, Hennekam RC. Oosterwijk JC, et al. J Med Genet. 2003 Dec;40(12):937-41. doi: 10.1136/jmg.40.12.937. J Med Genet. 2003. PMID: 14684694 Free PMC article. Review. No abstract available.

4

Lamin B-receptor mutations in Pelger-Huët anomaly.

Best S, Salvati F, Kallo J, Garner C, Height S, Thein SL, Rees DC. Best S, et al. Br J Haematol. 2003 Nov;123(3):542-4. doi: 10.1046/j.1365-2141.2003.04621.x. Br J Haematol. 2003. PMID: 14617022 Free article.

5

Pelger-Huet anomaly of leukocytes. Report of a case and survey of incidence.

LUDDEN TE, HARVEY M. LUDDEN TE, et al. Am J Clin Pathol. 1962 Mar;37:302-4. doi: 10.1093/ajcp/37.3.302. Am J Clin Pathol. 1962. PMID: 14467172 No abstract available.

6

The Pelger anomaly of leukocytes: forty-one cases in seven families.

SKENDZEL LP, HOFFMAN GC. SKENDZEL LP, et al. Am J Clin Pathol. 1962 Mar;37:294-301. doi: 10.1093/ajcp/37.3.294. Am J Clin Pathol. 1962. PMID: 13913617 No abstract available.

7

The Pelger-Huët anomaly in three families and its use in determining the disappearance of transfused neutrophils from the peripheral blood.

ROSSE WF, GURNEY CW. ROSSE WF, et al. Blood. 1959 Feb;14(2):170-86. Blood. 1959. PMID: 13618374 Free article. No abstract available.

8

Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene.

Waterham HR, Koster J, Mooyer P, Noort Gv Gv, Kelley RI, Wilcox WR, Wanders RJ, Hennekam RC, Oosterwijk JC. Waterham HR, et al. Am J Hum Genet. 2003 Apr;72(4):1013-7. doi: 10.1086/373938. Epub 2003 Feb 28. Am J Hum Genet. 2003. PMID: 12618959 Free PMC article.

9

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.

Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger C, Herrmann H, Kalscheuer V, Olins AL, Olins DE, Sperling K, Hoffmann K. Shultz LD, et al. Hum Mol Genet. 2003 Jan 1;12(1):61-9. doi: 10.1093/hmg/ddg003. Hum Mol Genet. 2003. PMID: 12490533

10

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly).

Hoffmann K, Dreger CK, Olins AL, Olins DE, Shultz LD, Lucke B, Karl H, Kaps R, Müller D, Vayá A, Aznar J, Ware RE, Sotelo Cruz N, Lindner TH, Herrmann H, Reis A, Sperling K. Hoffmann K, et al. Nat Genet. 2002 Aug;31(4):410-4. doi: 10.1038/ng925. Epub 2002 Jul 15. Nat Genet. 2002. PMID: 12118250

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