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Items: 1 to 20 of 212

2.

The acrocallosal syndrome in sisters.

Schinzel A, Kaufmann U.

Clin Genet. 1986 Nov;30(5):399-405.

PMID:
3802558
4.

The acrocallosal syndrome in a Turkish boy.

Yüksel M, Caliskan M, Oğur G, Ozmen M, Dolunay G, Apak S.

J Med Genet. 1990 Jan;27(1):48-9.

5.

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Brueton LA, Chotai KA, van Herwerden L, Schinzel A, Winter RM.

J Med Genet. 1992 Sep;29(9):635-7.

6.

Acrocallosal syndrome.

Shilpa BJ, Ashok L, Sattur PA.

J Indian Soc Pedod Prev Dent. 2006 Mar;24(1):45-9.

7.
8.
9.

Schinzel acrocallosal syndrome.

Gulati S, Menon S, Kabra M, Kalra V.

Indian J Pediatr. 2003 Feb;70(2):173-6.

PMID:
12661815
10.

An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.

Aykut A, Cogulu O, Ekmekci AY, Ozkinay F.

Genet Couns. 2008;19(2):237-40.

PMID:
18618999
11.

Diagnosing acrocallosal syndrome.

Gupta A, Thakur S, Phadke SR.

Indian J Pediatr. 2003 Feb;70(2):177-9.

PMID:
12661816
12.

Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.

Pfeiffer RA, Legat G, Trautmann U.

Ann Genet. 1992;35(1):41-6.

PMID:
1610119
13.

Agenesis of the corpus callosum and macrocephaly in siblings.

Young ID, Trounce JQ, Levene MI, Fitzsimmons JS, Moore JR.

Clin Genet. 1985 Sep;28(3):225-30.

PMID:
3905089
14.

Japanese kindred with FG syndrome.

Kato R, Niikawa N, Nagai T, Fukushima Y.

Am J Med Genet. 1994 Aug 15;52(2):242-3. No abstract available.

PMID:
7802020
15.

Two sisters with Toriello-Carey syndrome.

Chinen Y, Tohma T, Izumikawa Y, Taketomi H, Iha T, Ohta T, Naritomi K.

Am J Med Genet. 1999 Nov 26;87(3):262-4.

PMID:
10564882
16.

[Rudimentary acral anomalies in a patient with Acrocal-losal syndrome].

Silengo M, Del Monaco A, Defilippi C.

Radiol Med. 2001 Apr;101(4):299-301. Italian. No abstract available.

PMID:
11398065
17.

[Acrocallosal syndrome (Schinzel type)].

Matsuo M.

Ryoikibetsu Shokogun Shirizu. 2001;(33):113-4. Review. Japanese. No abstract available.

PMID:
11462356
18.

Corpus callosum agenesis in Coffin-Lowry syndrome.

Soekarman D, Fryns JP.

Genet Couns. 1994;5(1):77-80.

PMID:
8031540
19.

Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.

Zweier C, Temple IK, Beemer F, Zackai E, Lerman-Sagie T, Weschke B, Anderson CE, Rauch A.

J Med Genet. 2003 Aug;40(8):601-5. No abstract available.

20.

Schinzel acrocallosal syndrome: a variant example of the Greig syndrome?

Legius E, Fryns JP, Casaer P, Boel M, Eggermont E.

Ann Genet. 1985;28(4):239-40.

PMID:
3879437
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