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Results: 1 to 20 of 32

Related Articles by Review for PubMed (Select 8368246)

1.

Hypertrichosis, atrophic skin, ectropion, and macrostomia (Barber-Say syndrome): report of a new case.

Martínez Santana S, Pérez Alvarez F, Frías JL, Martínez-Frías ML.

Am J Med Genet. 1993 Aug 1;47(1):20-3.

PMID:
8368246
2.

[Barber-Say syndrome].

Makita Y.

Ryoikibetsu Shokogun Shirizu. 2001;(33):250. Review. Japanese. No abstract available.

PMID:
11462424
3.

Lid agenesis-macrostomia-psychomotor retardation-forehead hypertrichosis--a new syndrome?

Cesarino EJ, Pinheiro M, Freire-Maia N, Meira-Silva MC.

Am J Med Genet. 1988 Oct;31(2):299-304. Review.

PMID:
3068987
4.

A new feature of the ablepharon macrostomia syndrome: zygomatic arch absence.

Jackson IT, Shaw KE, del Pinal Matorras F.

Br J Plast Surg. 1988 Jul;41(4):410-6. Review.

PMID:
3293678
5.

Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: a new distinct entity.

Canún S, Guevara-Sanginés EG, Elvira-Morales A, Sierra-Romero Mdel C, Rodríguez-Asbun H.

Am J Med Genet A. 2003 Jan 30;116A(3):278-83. Review.

PMID:
12503107
6.

Coffin-Siris syndrome: a case of an extremely low birthweight infant with severe kyphoscoliosis.

Suzumura H, Sakurai K, Kano K, Ichimura T.

Acta Paediatr Jpn. 1996 Oct;38(5):537-40. Review.

PMID:
8942018
7.

Primary hypogonadism, partial alopecia, and Mullerian hypoplasia: report of a third family and review.

Tatar A, Ocak Z, Tatar A, Yesilyurt A, Borekci B, Oztas S.

Am J Med Genet A. 2009 Mar;149A(3):501-4. doi: 10.1002/ajmg.a.32645. Review.

PMID:
19213036
8.

Gingival overgrowth, congenital generalized hypertrichosis, mental retardation and epilepsy: case report and overview.

Douzgou S, Mingarelli R, Dallapiccola B.

Clin Dysmorphol. 2009 Oct;18(4):205-8. doi: 10.1097/MCD.0b013e32832dc393. Review.

PMID:
19625955
9.

An MCA/MR syndrome with hypocholesterolemia due to familial hypobetalipoproteinemia: report of a second patient with Nguyen syndrome.

Nakane T, Hayashibe H, Nakazawa S.

Am J Med Genet A. 2005 Sep 1;137A(3):305-7. Review.

PMID:
16088930
10.

New cases of Bohring-Opitz syndrome, update, and critical review of the literature.

Bohring A, Oudesluijs GG, Grange DK, Zampino G, Thierry P.

Am J Med Genet A. 2006 Jun 15;140(12):1257-63. Review.

PMID:
16691589
11.

Cerebro-oculo-nasal syndrome: another case and review of the literature.

Ercal D, Say B.

Clin Dysmorphol. 1998 Apr;7(2):139-41. Review.

PMID:
9571287
12.

Two new cases of Cumming syndrome confirming autosomal recessive inheritance.

Pérez del Río MJ, Fernández-Toral J, Madrigal B, González-González M, Ablanedo P, Herrero A.

Am J Med Genet. 1999 Feb 12;82(4):340-3. Review.

PMID:
10051169
13.

Ectrodactyly, ectodermal dysplasia, and cleft lip syndrome. Case report.

Seno H, Yanai A, Sugino H, Inoue M, Takei T, Miyake I.

Scand J Plast Reconstr Surg Hand Surg. 1996 Sep;30(3):227-30. Review.

PMID:
8885020
14.

Neu-Laxova syndrome: report of a case and comments.

Karimi-Nejad MH, Khajavi H, Gharavi MJ, Karimi-Nejad R.

Am J Med Genet. 1987 Sep;28(1):17-23. Review.

PMID:
3314507
15.

FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3].

Dessay S, Moizard MP, Gilardi JL, Opitz JM, Middleton-Price H, Pembrey M, Moraine C, Briault S.

Am J Med Genet. 2002 Sep 15;112(1):6-11. Review.

PMID:
12239712
16.

Toriello-Carey syndrome: delineation and review.

Toriello HV, Carey JC, Addor MC, Allen W, Burke L, Chun N, Dobyns W, Elias E, Gallagher R, Hordijk R, Hoyme G, Irons M, Jewett T, LeMerrer M, Lubinsky M, Martin R, McDonald-McGinn D, Neumann L, Newman W, Pauli R, Seaver L, Tsai A, Wargowsky D, Williams M, Zackai E.

Am J Med Genet A. 2003 Nov 15;123A(1):84-90. Review.

PMID:
14556252
17.

Hypertrichosis cubiti: two new cases and a review of the literature.

Visser R, Beemer FA, Veenhoven RH, De Nef JJ.

Genet Couns. 2002;13(4):397-403. Review.

PMID:
12558109
18.

Congenital melanosis and hypertrichosis in bilateral distribution.

Ferreira MJ, Bajanca R, Fiadeiro T.

Pediatr Dermatol. 1998 Jul-Aug;15(4):290-2. Review.

PMID:
9720695
19.

The triple risk hypotheses in sudden infant death syndrome.

Guntheroth WG, Spiers PS.

Pediatrics. 2002 Nov;110(5):e64. Review.

PMID:
12415070
20.

Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22)

Baumeister FA, Egger J, Schildhauer MT, Stengel-Rutkowski S.

Clin Genet. 1993 Sep;44(3):121-8. Review.

PMID:
8275569
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