Opitz JM - Search Results

1

Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome.

Neri G, Marini R, Cappa M, Borrelli P, Opitz JM. Neri G, et al. Among authors: opitz jm. Am J Med Genet. 1988 May-Jun;30(1-2):287-99. doi: 10.1002/ajmg.1320300130. Am J Med Genet. 1988. PMID: 3177455

2

Encomium and dedication: Angelo Serra--four decades in human and medical genetics.

Neri G, Opitz JM. Neri G, et al. Among authors: opitz jm. Am J Med Genet Suppl. 1990;7:5-8. Am J Med Genet Suppl. 1990. PMID: 2149973 No abstract available.

3

"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment.

Lalatta F, Clerici Bagozzi D, Salmoiraghi MG, Tagliabue P, Tischer C, Zollino M, Di Rocco C, Neri G, Opitz JM. Lalatta F, et al. Among authors: opitz jm. Am J Med Genet. 1990 Dec;37(4):451-6. doi: 10.1002/ajmg.1320370404. Am J Med Genet. 1990. PMID: 2260586

4

The Perlman syndrome: clinical and biological aspects.

Neri G, Martini-Neri ME, Opitz JM, Freed JJ. Neri G, et al. Among authors: opitz jm. Prog Clin Biol Res. 1985;200:269-76. Prog Clin Biol Res. 1985. PMID: 3001776 No abstract available.

5

FG syndrome update 1988: note of 5 new patients and bibliography.

Opitz JM, Richieri-da Costa A, Aase JM, Benke PJ. Opitz JM, et al. Am J Med Genet. 1988 May-Jun;30(1-2):309-28. doi: 10.1002/ajmg.1320300132. Am J Med Genet. 1988. PMID: 3052062 Review.

6

Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family.

Opitz JM, Herrmann J, Gilbert EF, Matalon R. Opitz JM, et al. Am J Med Genet. 1988 May-Jun;30(1-2):301-8. doi: 10.1002/ajmg.1320300131. Am J Med Genet. 1988. PMID: 3177456

7

Facial midline defect in the fetal alcohol syndrome: embryogenetic considerations in two clinical cases.

Neri G, Sammito V, Romano C, Sanfilippo S, Opitz JM. Neri G, et al. Among authors: opitz jm. Am J Med Genet. 1988 Mar;29(3):477-82. doi: 10.1002/ajmg.1320290302. Am J Med Genet. 1988. PMID: 3376992

8

New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndrome.

Reynolds JF, Neri G, Herrmann JP, Blumberg B, Coldwell JG, Miles PV, Opitz JM. Reynolds JF, et al. Among authors: opitz jm. Am J Med Genet. 1986 Nov;25(3):413-27. doi: 10.1002/ajmg.1320250303. Am J Med Genet. 1986. PMID: 3789005

9

An X-linked recessive basal ganglia disorder with mental retardation.

Laxova R, Brown ES, Hogan K, Hecox K, Opitz JM. Laxova R, et al. Among authors: opitz jm. Am J Med Genet. 1985 Aug;21(4):681-9. doi: 10.1002/ajmg.1320210409. Am J Med Genet. 1985. PMID: 4025396

10

The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies.

Neri G, Martini-Neri ME, Katz BE, Opitz JM. Neri G, et al. Among authors: opitz jm. Am J Med Genet. 1984 Sep;19(1):195-207. doi: 10.1002/ajmg.1320190120. Am J Med Genet. 1984. PMID: 6093533

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