Cappa M - Search Results

1

Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.

Gurrieri F, Cappa M, Neri G. Gurrieri F, et al. Among authors: cappa m. Am J Med Genet. 1992 Sep 15;44(2):136-7. doi: 10.1002/ajmg.1320440203. Am J Med Genet. 1992. PMID: 1456280

2

The Opitz syndrome: a new designation for the clinically indistinguishable BBB and G syndromes.

Cappa M, Borrelli P, Marini R, Neri G. Cappa M, et al. Am J Med Genet. 1987 Oct;28(2):303-9. doi: 10.1002/ajmg.1320280207. Am J Med Genet. 1987. PMID: 2827473

3

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: cappa m. Am J Med Genet. 1988 May-Jun;30(1-2):287-99. doi: 10.1002/ajmg.1320300130. Am J Med Genet. 1988. PMID: 3177455

4

Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.

Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini R, Scarano G, Cappa M, Neri G. Zollino M, et al. Among authors: cappa m. Am J Med Genet. 1994 Sep 1;52(3):302-7. doi: 10.1002/ajmg.1320520310. Am J Med Genet. 1994. PMID: 7810561

5

Nonsyndromal overgrowth in males with mild psychomotor delay.

Neri G, Steindl K, Mazzei A, Battaglia A, Cappa M. Neri G, et al. Among authors: cappa m. Am J Med Genet. 1998 Oct 2;79(4):291-3. Am J Med Genet. 1998. PMID: 9781910

6

Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome. 1988.

Neri G, Marini R, Cappa M, Borrelli P, Opitz JM. Neri G, et al. Among authors: cappa m. Am J Med Genet A. 2013 Nov;161A(11):2697-703. doi: 10.1002/ajmg.a.36317. Am J Med Genet A. 2013. PMID: 24166811

7

Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome.

Schwartz CE, Gillessen-Kaesbach G, May M, Cappa M, Gorski J, Steindl K, Neri G. Schwartz CE, et al. Among authors: cappa m. Eur J Hum Genet. 2000 Nov;8(11):869-74. doi: 10.1038/sj.ejhg.5200553. Eur J Hum Genet. 2000. PMID: 11093277

8

The growth hormone response to hexarelin in patients with Prader-Willi syndrome.

Cappa M, Raguso G, Palmiotto T, Faedda A, Gurreri F, Neri G, Deghenghi R, Loche S. Cappa M, et al. J Endocrinol Invest. 1998 Sep;21(8):501-5. doi: 10.1007/BF03347335. J Endocrinol Invest. 1998. PMID: 9801990

9

Cutis verticis gyrata and chromosomal abnormalities.

Marini R, Cappa M, Neri G. Marini R, et al. Among authors: cappa m. Am J Dis Child. 1989 Mar;143(3):269-70. Am J Dis Child. 1989. PMID: 2916502 No abstract available.

10

Clinical and roentgenographic findings in a patient with primordial microcephalic dwarfism type Caroline Crachami.

Boscherini B, Colabucci F, Galasso C, Marietti G, Cappa M, Pasquino AM. Boscherini B, et al. Among authors: cappa m. Am J Med Genet. 1996 Dec 18;66(3):269-72. doi: 10.1002/(SICI)1096-8628(19961218)66:3<269::AID-AJMG6>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8985485

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