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De novo translocation (8;12) and frontofacionasal dysplasia in a newborn boy.
Am J Med Genet. 2000 Sep 18;94(3):179-83. doi: 10.1002/1096-8628(20000918)94:3<179::aid-ajmg1>3.0.co;2-n.
Am J Med Genet. 2000.
PMID: 10995502
Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
Habecker-Green JG, Naeem R, Gold H, O'Grady JP, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn GM.
Habecker-Green JG, et al.
J Perinatol. 1998 Sep-Oct;18(5):395-8.
J Perinatol. 1998.
PMID: 9766419
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Reproduction in a patient with trisomy 8 mosaicism: case report and literature review.
Habecker-Green J, Naeem R, Goh W, Pflueger S, Murray M, Cohn G.
Habecker-Green J, et al.
Am J Med Genet. 1998 Feb 3;75(4):382-5.
Am J Med Genet. 1998.
PMID: 9482643
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The usefulness of a prenatal genetic questionnaire in genetic risk assessment.
Cohn GM, Cimaroli T, Gould M, Macri CJ, Habecker-Green J, Miller RC.
Cohn GM, et al. Among authors: habecker green j.
Obstet Gynecol. 1996 Nov;88(5):806-10. doi: 10.1016/0029-7844(96)00284-0.
Obstet Gynecol. 1996.
PMID: 8885918
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The importance of genetic counseling before amniocentesis.
Cohn GM, Gould M, Miller RC, Habecker-Green J, Macri CJ, Gimovsky ML.
Cohn GM, et al. Among authors: habecker green j.
J Perinatol. 1996 Sep-Oct;16(5):352-7; quiz 358-9.
J Perinatol. 1996.
PMID: 8915933
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