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Items: 1 to 20 of 133

1.

Congenital universal alopecia, mental deficiency, and microcephaly in two sibs.

Pfeiffer RA, Völklein J.

J Med Genet. 1982 Oct;19(5):388-9. No abstract available.

2.

A familial syndrome of microcephaly, sparse hair, mental retardation, and seizures.

van Haeringen A, Hurst JA, Savidge R, Baraitser M.

J Med Genet. 1990 Feb;27(2):127-9.

3.

Alopecia, mental retardation, epilepsy and microcephaly in two cousins.

Pridmore C, Baraitser M, Brett EM.

Clin Dysmorphol. 1992 Apr;1(2):79-84.

PMID:
1345516
4.

Alopecia/mental retardation syndrome.

Hannig VL, Tiller GE.

Am J Med Genet. 1995 Aug 28;58(2):123-4. Review.

PMID:
8533801
5.

Congenital alopecia, seizures, and psychomotor retardation in three siblings.

Wessel HB, Barmada MA, Hashida Y.

Pediatr Neurol. 1987 Mar-Apr;3(2):101-7. Review.

PMID:
3334010
7.

X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.

Lungarotti MS, Martello C, Barboni G, Mezzetti D, Mariotti G, Calabro A.

Am J Med Genet. 1994 Jul 15;51(4):598-601. Review.

PMID:
7943046
8.

Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndrome.

Harbord MG, Baraitser M, Wilson J.

J Med Genet. 1989 Jun;26(6):397-400.

9.
10.

Congenital alopecia, psychomotor retardation, convulsions in two sibs of a consanguineous marriage.

Perniola T, Krajewska G, Carnevale F, Lospalluti M.

J Inherit Metab Dis. 1980;3(2):49-53.

PMID:
6777601
11.

Expanding the phenotype of alopecia-contractures-dwarfism mental retardation syndrome (ACD syndrome): description of an additional case and review of the literature.

Schell-Apacik C, Hardt M, Ertl-Wagner B, Klopocki E, Möhrenschlager M, Heinrich U, von Voss H.

Eur J Pediatr. 2008 Sep;167(9):1057-62. doi: 10.1007/s00431-007-0641-6. Epub 2008 Jan 17. Review.

PMID:
18204861
12.

Sporadic trichodental dysplasia with microcephaly and mental retardation.

Giannotti A, Digilio MC, Albertini G, Mingarelli R, Dallapiccola B.

Clin Dysmorphol. 1995 Oct;4(4):334-7.

PMID:
8574424
13.
14.

Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?

Steijlen PM, Neumann HA, der Kinderen DJ, Smeets DF, van der Kerkhof PC, Happle R.

J Am Acad Dermatol. 1994 May;30(5 Pt 2):893-8. Review.

PMID:
8169270
15.

Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: "D-CHRAMPS syndrome".

Hiyasat D, Dehyyat MA, Ajlouni S, Mubaidin AF, Till M, Hadidi A, El-Shanti H, Ajlouni KM.

Eur J Pediatr. 2002 Mar;161(3):170-2.

PMID:
11998919
16.

Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.

Garty BZ, Eisenstein B, Sandbank J, Kaffe S, Dagan R, Gadoth N.

J Med Genet. 1994 Feb;31(2):121-5.

18.

Letter: Universal alopecia and microcephaly in 4 siblings.

Mosavy SH.

S Afr Med J. 1975 Feb 8;49(6):172. No abstract available.

PMID:
1124456
19.
20.

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
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