Barbi G - Search Results

1

Eradication of a dysfunctional HLA-haploidentical T cell system by a second HLA-identical BMT.

Ege M, Manfras BJ, Barbi G, Schulz AS, Sigl-Kraetzig M, Debatin KM, Friedrich W, Mueller SM. Ege M, et al. Among authors: barbi g. Bone Marrow Transplant. 2001 Nov;28(10):993-5. doi: 10.1038/sj.bmt.1703263. Bone Marrow Transplant. 2001. PMID: 11753558

2

ICF syndrome: high variability of the chromosomal phenotype and association with classical Hodgkin lymphoma.

Schuetz C, Barbi G, Barth TF, Hoenig M, Schulz A, Möeller P, Smeets D, de Greef JC, van der Maarel SM, Vogel W, Debatin KM, Friedrich W. Schuetz C, et al. Among authors: barbi g. Am J Med Genet A. 2007 Sep 1;143A(17):2052-7. doi: 10.1002/ajmg.a.31885. Am J Med Genet A. 2007. PMID: 17702009

3

Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.

Gläser B, Rossier E, Barbi G, Chiaie LD, Blank C, Vogel W, Kehrer-Sawatzki H. Gläser B, et al. Among authors: barbi g. Am J Med Genet A. 2003 Jan 1;116A(1):66-70. doi: 10.1002/ajmg.a.10878. Am J Med Genet A. 2003. PMID: 12476454 Review.

4

False-negative findings in chorionic villus sampling. An experimental approach and review of the literature.

Kennerknecht I, Barbi G, Djalali M, Mehnert K, Schneider M, Terinde R, Vogel W. Kennerknecht I, et al. Among authors: barbi g. Prenat Diagn. 1998 Dec;18(12):1276-82. Prenat Diagn. 1998. PMID: 9885019 Review.

5

Xp-duplications with and without sex reversal.

Baumstark A, Barbi G, Djalali M, Geerkens C, Mitulla B, Mattfeldt T, de Almeida JC, Vargas FR, Llerena Júnior JC, Vogel W, Just W. Baumstark A, et al. Among authors: barbi g. Hum Genet. 1996 Jan;97(1):79-86. doi: 10.1007/BF00218838. Hum Genet. 1996. PMID: 8557267 Review.

6

Maternal transmission of ring chromosome 21.

Kennerknecht I, Barbi G, Vogel W. Kennerknecht I, et al. Among authors: barbi g. Hum Genet. 1990 Nov;86(1):99-101. doi: 10.1007/BF00205185. Hum Genet. 1990. PMID: 2253944

7

XX-agonadism in a fetus with multiple dysraphic lesions: a new syndrome.

Kennerknecht I, Mattfeldt T, Paulus W, Nitsch C, Negri G, Barbi G, Just W, Schwemmle S, Vogel W. Kennerknecht I, et al. Among authors: barbi g. Am J Med Genet. 1997 Jun 27;70(4):413-4. Am J Med Genet. 1997. PMID: 9182784

8

Uncommon chromosomal mosaicism in chorionic villi.

Kennerknecht I, Barbi G, Djalali M, Just W, Vogel W, Terinde R. Kennerknecht I, et al. Among authors: barbi g. Prenat Diagn. 1991 Aug;11(8):569-75. doi: 10.1002/pd.1970110813. Prenat Diagn. 1991. PMID: 1766932

9

Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype.

Barbi G, Kennerknecht I, Wöhr G, Avramopoulos D, Karadima G, Petersen MB. Barbi G, et al. Am J Med Genet. 2000 Mar 13;91(2):116-22. doi: 10.1002/(sici)1096-8628(20000313)91:2<116::aid-ajmg7>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10748409

10

Cytogenetic diagnoses after chorionic villus sampling are less reliable in very-high-or very-low-risk pregnancies.

Kennerknecht I, Barbi G, Wolf M, Djalali M, Grab D, Terinde R, Vogel W. Kennerknecht I, et al. Among authors: barbi g. Prenat Diagn. 1993 Oct;13(10):929-44. doi: 10.1002/pd.1970131007. Prenat Diagn. 1993. PMID: 8309900

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