Mehraein Y - Search Results

1

A new familial case of microdeletion syndrome 10p15.3.

Eggert M, Müller S, Heinrich U, Mehraein Y. Eggert M, et al. Among authors: mehraein y. Eur J Med Genet. 2016 Apr;59(4):179-82. doi: 10.1016/j.ejmg.2016.02.008. Epub 2016 Feb 24. Eur J Med Genet. 2016. PMID: 26921531

2

2q37.3 Deletion Syndrome: Two Cases with Highly Distinctive Facial Phenotype, Discordant Association with Schizophrenic Psychosis, and Shared Deletion Breakpoint Region on 2q37.3.

Mehraein Y, Pfob M, Steinlein O, Aichinger E, Eggert M, Bubendorff V, Mannhart A, Müller S. Mehraein Y, et al. Cytogenet Genome Res. 2015;146(1):33-8. doi: 10.1159/000431389. Epub 2015 Jun 19. Cytogenet Genome Res. 2015. PMID: 26112830

3

DICER1 syndrome can mimic different genetic tumor predispositions.

Mehraein Y, Schmid I, Eggert M, Kohlhase J, Steinlein OK. Mehraein Y, et al. Cancer Lett. 2016 Jan 28;370(2):275-8. doi: 10.1016/j.canlet.2015.11.002. Epub 2015 Nov 11. Cancer Lett. 2016. PMID: 26577641

4

A non-coding mutation in the 5' untranslated region of patched homologue 1 predisposes to basal cell carcinoma.

Tietze JK, Pfob M, Eggert M, von Preußen A, Mehraein Y, Ruzicka T, Herzinger T. Tietze JK, et al. Among authors: mehraein y. Exp Dermatol. 2013 Dec;22(12):834-5. doi: 10.1111/exd.12267. Exp Dermatol. 2013. PMID: 24131384

5

Microdeletion 22q11 in complex cardiovascular malformations.

Mehraein Y, Wippermann CF, Michel-Behnke I, Nhan Ngo TK, Hillig U, Giersberg M, Aulepp U, Barth H, Fritz B, Rehder H. Mehraein Y, et al. Hum Genet. 1997 Apr;99(4):433-42. doi: 10.1007/s004390050385. Hum Genet. 1997. PMID: 9099830

6

Somatic mosaicism of chromosome 7 in a highly proliferating melanocytic congenital naevus in a ring chromosome 7 patient.

Mehraein Y, Ehlhardt S, Wagner A, Göttert E, Tilgen W, Zang KD, Dill-Müller D. Mehraein Y, et al. Am J Med Genet A. 2004 Dec 1;131(2):179-85. doi: 10.1002/ajmg.a.30370. Am J Med Genet A. 2004. PMID: 15523614

7

Search for deletion 22q11.2 in interphase nuclei of buccal mucosa of patients ascertained by isolated cleft palate: a new diagnostic approach.

Shouman N, Pabst B, Arslan-Kirchner M, Eckardt A, Schönweiler R, Ptok M, Mehraein Y, Schmidtke J, Miller K. Shouman N, et al. Among authors: mehraein y. Int J Oral Maxillofac Surg. 2003 Apr;32(2):198-200. doi: 10.1054/ijom.2002.0336. Int J Oral Maxillofac Surg. 2003. PMID: 12729782

8

Detection of sex chromosomal aneuploidies X-X, Y-Y, and X-Y in human sperm using two-chromosome fluorescence in situ hybridization.

Wyrobek AJ, Robbins WA, Mehraein Y, Pinkel D, Weier HU. Wyrobek AJ, et al. Among authors: mehraein y. Am J Med Genet. 1994 Oct 15;53(1):1-7. doi: 10.1002/ajmg.1320530102. Am J Med Genet. 1994. PMID: 7802028

9

Hand malformations in the aborted embryo: an important source of genetic information.

Ramsing M, Duda V, Mehraein Y, Gruber H, Coerdt W, Holzgreve W, Rehder H. Ramsing M, et al. Among authors: mehraein y. Birth Defects Orig Artic Ser. 1996;30(1):79-94. Birth Defects Orig Artic Ser. 1996. PMID: 9125349 No abstract available.

10

[Diagnosis of fetal virus infections by in situ hybridization].

Mehraein Y, Rehder H, Draeger HG, Froster-Iskenius UG, Schwinger E, Holzgreve W. Mehraein Y, et al. Geburtshilfe Frauenheilkd. 1991 Dec;51(12):984-9. doi: 10.1055/s-2008-1026249. Geburtshilfe Frauenheilkd. 1991. PMID: 1665465 German.

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