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Results: 13

Related Articles by Review for PubMed (Select 21815250)

1.

The microcephaly-capillary malformation syndrome.

Mirzaa GM, Paciorkowski AR, Smyser CD, Willing MC, Lind AC, Dobyns WB.

Am J Med Genet A. 2011 Sep;155A(9):2080-7. doi: 10.1002/ajmg.a.34118. Epub 2011 Aug 3.

2.

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
3.

Filippi syndrome: report of three additional cases.

Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.

Am J Med Genet. 1999 Nov 19;87(2):128-33. Review.

PMID:
10533026
4.

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
5.

Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?

Janssen HC, Schaap C, Vandevijver N, Moerman P, de Die-Smulders CE, Fryns JP.

J Med Genet. 1999 Jun;36(6):481-4. Review.

6.

Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy.

Cooperstone BG, Friedman A, Kaplan BS.

Am J Med Genet. 1993 Aug 15;47(2):250-4. Review.

PMID:
8213914
7.
9.

Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.

Nakata NM, Guion-Almeida ML, Richieri-Costa A.

Am J Med Genet. 1993 Sep 1;47(3):330-2. Review.

PMID:
8135276
10.

Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology.

Zampino G, Mastroiacovo P, Ricci R, Zollino M, Segni G, Martini-Neri ME, Neri G.

Am J Med Genet. 1993 Aug 15;47(2):176-83. Review.

PMID:
8213903
11.

Feingold syndrome: report of a new family and review.

Courtens W, Levi S, Verbelen F, Verloes A, Vamos E.

Am J Med Genet. 1997 Nov 28;73(1):55-60. Review.

PMID:
9375923
12.

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
13.
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