Cohen M - Search Results

1

Multiplex-FISH for pre- and postnatal diagnostic applications.

Uhrig S, Schuffenhauer S, Fauth C, Wirtz A, Daumer-Haas C, Apacik C, Cohen M, Müller-Navia J, Cremer T, Murken J, Speicher MR. Uhrig S, et al. Among authors: cohen m. Am J Hum Genet. 1999 Aug;65(2):448-62. doi: 10.1086/302508. Am J Hum Genet. 1999. PMID: 10417288 Free PMC article.

2

Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the mother.

Apacik C, Cohen M, Jakobeit M, Schmucker B, Schuffenhauer S, Thurn und Taxis E, Genzel-Boroviczeny O, Stengel-Rutkowski S. Apacik C, et al. Among authors: cohen m. Clin Genet. 1996 Aug;50(2):63-73. doi: 10.1111/j.1399-0004.1996.tb02350.x. Clin Genet. 1996. PMID: 8937763 Review.

3

Multicolour FISH fine mapping unravels an insertion as a complex chromosomal rearrangement involving six breakpoints and a 5.89 Mb large deletion.

Kraus J, Cohen M, Speicher MR. Kraus J, et al. Among authors: cohen m. J Med Genet. 2003 May;40(5):e60. doi: 10.1136/jmg.40.5.e60. J Med Genet. 2003. PMID: 12746414 Free PMC article. No abstract available.

4

Single mandibular incisor in a patient with del (18p) anomaly.

Pfeiffer RA, Hertrich K, Cohen M. Pfeiffer RA, et al. Among authors: cohen m. Clin Genet. 1994 Dec;46(6):430-2. doi: 10.1111/j.1399-0004.1994.tb04411.x. Clin Genet. 1994. PMID: 7889660

5

A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies.

Kline AD, Griffin CA, Haddadin MH, Chudoba I, Morsberger LA, Hawkins AL, Amato RS, Munshi G, Cohen MM. Kline AD, et al. Among authors: cohen mm. Am J Med Genet A. 2004 Aug 30;129A(2):124-9. doi: 10.1002/ajmg.a.30130. Am J Med Genet A. 2004. PMID: 15316975

6

[Sjögren-Larsson syndrome].

Möhrenschlager M, Rizzo WB, Kraus CS, Limbrock J, Cohen M, Anton-Lamprecht I, Abeck D, Ring J. Möhrenschlager M, et al. Among authors: cohen m. Hautarzt. 2000 Apr;51(4):250-5. doi: 10.1007/s001050051113. Hautarzt. 2000. PMID: 10810660 German.

7

[Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].

Briegel W, Cohen M. Briegel W, et al. Among authors: cohen m. Z Kinder Jugendpsychiatr Psychother. 2004 May;32(2):107-15. doi: 10.1024/1422-4917.32.2.107. Z Kinder Jugendpsychiatr Psychother. 2004. PMID: 15181786 Review. German.

8

An Analysis of the Association of Whole Blood Transfusion With the Development of Acute Respiratory Distress Syndrome.

Moreno AR, Fisher AD, Long BJ, Douin DJ, Wright FL, Rizzo JA, April MD, Cohen MJ, Getz TM, Schauer SG. Moreno AR, et al. Among authors: cohen mj. Crit Care Med. 2025 Jan 1;53(1):e109-e116. doi: 10.1097/CCM.0000000000006477. Epub 2024 Nov 15. Crit Care Med. 2025. PMID: 39774204

9

An Analysis of the Association of Whole Blood Transfusion With the Development of Acute Respiratory Distress Syndrome.

Moreno AR, Fisher AD, Long BJ, Douin DJ, Wright FL, Rizzo JA, April MD, Cohen MJ, Getz TM, Schauer SG. Moreno AR, et al. Among authors: cohen mj. Crit Care Med. 2024 Nov 15. doi: 10.1097/CCM.0000000000006477. Online ahead of print. Crit Care Med. 2024. PMID: 39773781

10

Gender, Racial, and Fitzpatrick Skin Type Representation in Melasma Clinical Trials.

Wang JY, Zafar K, Bitterman D, Patel P, Kabakova M, Cohen M, Jagdeo J. Wang JY, et al. Among authors: cohen m. J Drugs Dermatol. 2025 Jan 1;24(1):19-22. doi: 10.36849/JDD.8379. J Drugs Dermatol. 2025. PMID: 39761136

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