Hirsch B - Search Results

1

Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome.

Reish O, Berry SA, Hirsch B. Reish O, et al. Among authors: hirsch b. Am J Med Genet. 1995 Dec 4;59(4):467-75. doi: 10.1002/ajmg.1320590413. Am J Med Genet. 1995. PMID: 8585567

2

Infant with multiple congenital anomalies and deletion (9)(q34.3).

Schimmenti LA, Berry SA, Tuchman M, Hirsch B. Schimmenti LA, et al. Among authors: hirsch b. Am J Med Genet. 1994 Jun 1;51(2):140-2. doi: 10.1002/ajmg.1320510211. Am J Med Genet. 1994. PMID: 7522397

3

Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.

Hirsch B, Baldinger S. Hirsch B, et al. Am J Med Genet. 1993 Jan 1;45(1):5-8. doi: 10.1002/ajmg.1320450104. Am J Med Genet. 1993. PMID: 8418660

4

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, Harding BN, Andermann E, Abdullah R, Berg M, Czapansky-Bielman D, Flanders DJ, Guerrini R, Motté J, Mira AP, Scheffer I, Berkovic S, Scaravilli F, King RA, Ledbetter DH, Schlessinger D, Dobyns WB, Walsh CA. Ross ME, et al. Among authors: hirsch b. Hum Mol Genet. 1997 Apr;6(4):555-62. doi: 10.1093/hmg/6.4.555. Hum Mol Genet. 1997. PMID: 9097958

5

Mosaicism for deletion 1p36.33 in a patient with obesity and hyperphagia.

Eugster EA, Berry SA, Hirsch B. Eugster EA, et al. Among authors: hirsch b. Am J Med Genet. 1997 Jun 27;70(4):409-12. doi: 10.1002/(sici)1096-8628(19970627)70:4<409::aid-ajmg14>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9182783

6

Toward quality assurance for metaphase FISH: a multicenter experience.

Dewald GW, Stallard R, Bader PI, Chen K, Zenger-Hain J, Harris CJ, Higgins R, Hirsch B, Hsu WT, Johnson E, Kubic V, Kurczynski TW, Malone JM, McCorquodale DJ, Meilinger K, Meisner LF, Moore JW, Schwartz S, Siembieda S, Storto PD, Vance G, Van Tuinen P, Wiktor A, Yung JF. Dewald GW, et al. Among authors: hirsch b. Am J Med Genet. 1996 Oct 28;65(3):190-6. doi: 10.1002/(SICI)1096-8628(19961028)65:3<190::AID-AJMG4>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 9240742

7

Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia.

Fink JM, Dobyns WB, Guerrini R, Hirsch BA. Fink JM, et al. Among authors: hirsch ba. Am J Hum Genet. 1997 Aug;61(2):379-87. doi: 10.1086/514863. Am J Hum Genet. 1997. PMID: 9311743 Free PMC article.

8

A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators.

Raymond CS, Parker ED, Kettlewell JR, Brown LG, Page DC, Kusz K, Jaruzelska J, Reinberg Y, Flejter WL, Bardwell VJ, Hirsch B, Zarkower D. Raymond CS, et al. Among authors: hirsch b. Hum Mol Genet. 1999 Jun;8(6):989-96. doi: 10.1093/hmg/8.6.989. Hum Mol Genet. 1999. PMID: 10332030

9

Unbalanced 4;6 translocation and progressive renal disease.

Pierpont ME, Hentges AS, Gears LJ, Hirsch B, Sinaiko A. Pierpont ME, et al. Among authors: hirsch b. Am J Med Genet. 2000 Nov 27;95(3):275-80. Am J Med Genet. 2000. PMID: 11102935

10

Paris-Trousseau syndrome platelets in a child with Jacobsen's syndrome.

Krishnamurti L, Neglia JP, Nagarajan R, Berry SA, Lohr J, Hirsch B, White JG. Krishnamurti L, et al. Among authors: hirsch b. Am J Hematol. 2001 Apr;66(4):295-9. doi: 10.1002/ajh.1061. Am J Hematol. 2001. PMID: 11279643 Free article.

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