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Items: 1 to 20 of 106

1.

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly.

Münke M.

Am J Med Genet. 1989 Oct;34(2):237-45. Review. No abstract available.

PMID:
2683787
2.

Holoprosencephaly: a developmental field defect.

Johnson VP.

Am J Med Genet. 1989 Oct;34(2):258-64.

PMID:
2629725
3.

Holoprosencephaly and cytogenetic findings: further information.

Cohen MM Jr.

Am J Med Genet. 1989 Oct;34(2):265. No abstract available.

PMID:
2817008
4.

Holoprosencephaly and interstitial deletion of 2(p2101p2109).

Wilson WG, Shanks DE, Sudduth KW, Couper KA, McIlhenny J.

Am J Med Genet. 1989 Oct;34(2):252-4.

PMID:
2817006
5.

Familial agnathia-holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance.

Krassikoff N, Sekhon GS.

Am J Med Genet. 1989 Oct;34(2):255-7. No abstract available.

PMID:
2817007
6.

[Median cleft face syndrome associated with holoprosencephaly. Description of a case].

de Toni T, Lazzaroni-Fossati F, Gastaldi R, Taccone A, Pesce F, Piccotti E, Balzarini C, Tarateta A.

Minerva Pediatr. 1985 Nov 30;37(21-22):875-82. Italian. No abstract available.

PMID:
4094605
7.

Cerebral midline developmental anomalies: spectrum and associated features.

Delezoide AL, Narcy F, Larroche JC.

Genet Couns. 1990;1(3-4):197-210. Review.

PMID:
2098044
8.

Holoprosencephaly in Border Leicester lambs.

Roth IJ, Morrow CJ, Wilkins JF, Harper PA.

Aust Vet J. 1987 Sep;64(9):271-3.

PMID:
3426465
9.

[Fatal genetic-morphologic syndromes. The campomelic syndrome].

Henkel KE, Pfeiffer RA, Stöss H.

Pathologe. 1993 May;14(3):162-4. German. No abstract available.

PMID:
8516273
10.

Agnathia, holoprosencephaly, and situs inversus.

Robinson HB Jr, Lenke R.

Am J Med Genet. 1989 Oct;34(2):266-7. No abstract available.

PMID:
2817009
11.

Autosomal dominant inheritance of the DeMyer Sequence.

Jaramillo C, Brandt SK, Jorgenson RJ.

J Craniofac Genet Dev Biol. 1988;8(3):199-204.

PMID:
3209682
12.

[Holoprosencephaly. Presentation of a case and review of the literature].

Naccari-Carlizzi M, Fedi M, Ravera G, Bartoli D, Gramegna M, Cottafava F.

Minerva Pediatr. 1987 May 15;39(9):371-6. Italian. No abstract available.

PMID:
3627067
13.

Fraser syndrome: prenatal ultrasonic detection.

Serville F, Carles D, Broussin B.

Am J Med Genet. 1989 Apr;32(4):561-3. No abstract available.

PMID:
2672816
14.

Acalvaria, holoprosencephaly, and facial dysmorphism syndrome.

Sperber GH, Honoré LH, Johnson ES.

J Craniofac Genet Dev Biol Suppl. 1986;2:319-29.

PMID:
3491120
15.

[Genetic morphologic fatal syndromes. Neu-Laxova syndrome].

Henkel KE, Pfeiffer RA, Stöss H.

Pathologe. 1993 Sep;14(5):271-3. German. No abstract available.

PMID:
8415438
16.

Further delineation of the Yunis-Varon syndrome.

Hennekam RC, Vermeulen-Meiners C.

J Med Genet. 1989 Jan;26(1):55-8.

17.

Lethal malformation syndrome in three siblings. A variable expression of the same entity?

Van Regemorter N, Pierquin G, Vamos E, Elmer C, Fryns JP.

Genet Couns. 1992;3(2):121-5. No abstract available.

PMID:
1642811
18.

Terminal 7q deletion as a cause of holoprosencephaly.

Masuno M, Orii T.

Clin Genet. 1990 Mar;37(3):238. No abstract available.

PMID:
2323097
19.

Pathological case of the month. Fetal brain disruption sequence.

DeJonge M, Poulik J.

Arch Pediatr Adolesc Med. 1997 Dec;151(12):1267-8. No abstract available.

PMID:
9412608
20.

Trisomy for the distal part of the short arm of chromosome 3.

Lurie IW, Korotkova IA, Zaletajev DV, Smirnova LI, Podlechshuk LV, Gurevich DB.

Helv Paediatr Acta. 1986 Mar;41(6):509-13.

PMID:
3583774
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