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Items: 1 to 20 of 190

1.

[Hypochondroplasia and mental retardation].

Rodríguez Delgado J, Guerrero Fernández J, Gracia Bouthelier R.

An Pediatr (Barc). 2008 Jun;68(6):629-32. Spanish. No abstract available.

2.

Skeletal dysplasias and mental retardation.

Chen H.

Prog Clin Biol Res. 1982;104:451-85. Review. No abstract available.

PMID:
6761697
3.

[Mental retardation and dyschondroplasia in four year old girl].

HEUYER G, MISES R, LOTE J, FLOURNOY O.

Arch Fr Pediatr. 1956;13(2):169-73. French. No abstract available.

PMID:
13328188
4.

[A new form of metaphyseal chondrodysplasia].

Khaldi F, Bennaceur B, Hamza M.

Arch Fr Pediatr. 1987 Feb;44(2):115-7. French.

PMID:
3579465
5.

Asphyxiating thoracic dysplasia as a complication of metaphyseal chondrodysplasia (Jansen type).

Ozonoff MB.

Birth Defects Orig Artic Ser. 1974;10(12):72-7. No abstract available.

PMID:
4461094
6.

Achondroplasia-hypochondroplasia complex.

Sommer A, Young-Wee T, Frye T.

Am J Med Genet. 1987 Apr;26(4):949-57.

PMID:
3591840
7.

Dyschondrosteosis associated with endocrine dysfunctions and mental deficiency.

Oikawa K, Yamaguchi T, Kato K, Takenouchi T, Yasuda K.

Tohoku J Exp Med. 1974 Nov;114(3):287-94. No abstract available.

8.

Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia.

Heinz-Erian P, Schmidt H, Le Merrer M, Phillips AD, Kiess W, Hadorn HB.

J Pediatr Gastroenterol Nutr. 1999 Feb;28(2):203-5. No abstract available.

PMID:
9932857
9.

Tricho-rhino-phalangeal type I syndrome and mental retardation: identification of a novel mutation in the TRPS1 gene.

Gonzalez-Huerta LM, Cuevas-Covarrubias SA, Messina-Baas OM.

J Dermatol Sci. 2007 Oct;48(1):61-3. Epub 2007 Aug 3. No abstract available.

PMID:
17689056
10.

Metaphyseal chondrodysplasias.

Spranger JW.

Birth Defects Orig Artic Ser. 1976;12(6):33-46. Review. No abstract available.

PMID:
788811
11.

Comparisons and correlations of skeletal defects in mouse and human.

Rimoin DL, Eteson DJ, Sillence DO.

Pathol Immunopathol Res. 1988;7(1-2):139-45. No abstract available.

PMID:
3222202
12.

[Hypochondroplasia due to the N540K mutation].

Bardallo Cruzado L, Bermúdez de la Vega JA, Jiménez Tejada M.

An Pediatr (Barc). 2006 Apr;64(4):393-4. Spanish. No abstract available.

13.

Unique survival in chrondrodysplasia-hermaphrodism syndrome.

Thauvin-Robinet C, Mugneret F, Callier P, Chouchane M, Garron E, Manceau E, Laurent N, Durand C, Nivelon-Chevallier A, Sapin E, Huet F, Faivre L.

Am J Med Genet A. 2005 Jan 30;132A(3):335-7. No abstract available.

PMID:
15578577
14.

Pulmonary embolism--a rare complication of Schimke immunoosseous dysplasia.

Sauerstein K, Schroth M, Amann K, Hoyer J, Singer H, Rauch A, Dötsch J.

Eur J Pediatr. 2007 Dec;166(12):1285-8. Epub 2006 Dec 29. No abstract available.

PMID:
17195070
15.

[Hypochondroplasia in children and its effect on growth and development].

Rybakowa M, Barylak A.

Endokrynol Pol. 1972 Sep-Oct;23(5):493-502. Polish. No abstract available.

PMID:
4642932
16.

[Supravalvular aortic stenosis, mental retardation and peculiar facies].

Guay JM, Dorion M, Roy M.

Union Med Can. 1968 Dec;97(12):1811-6. French. No abstract available.

PMID:
5746576
17.

[Familial mitochondrial myopathy with eczema and mental retardation].

Stoll C, Fischbach M, Walter PR, Lévy JM.

Pediatrie. 1980 Jul-Aug;35(5):419-24. French. No abstract available.

PMID:
7422449
18.

[Aspartylglucosaminuria: a point mutation as a cause of mental defect].

Ikonen E, Palotie L.

Duodecim. 1994;110(7):667-73. Review. Finnish. No abstract available.

PMID:
8542821
19.

Chondrodysplasia epiphysalis multiplex with diabetes mellitus and mental retardation.

NORMAN AP.

Proc R Soc Med. 1961 Apr;54:333-5. No abstract available.

20.

Advances in management of thalassemia.

Agarwal MB.

Indian J Pediatr. 2009 Feb;76(2):177-84. doi: 10.1007/s12098-009-0048-7. Epub 2009 Mar 28.

PMID:
19330306
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