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Results: 1 to 20 of 25

Related Articles by Review for PubMed (Select 8510994)

1.

Clinical diagnosis of genetic diseases.

Fong CT.

Pediatr Ann. 1993 May;22(5):277-81. Review. No abstract available.

PMID:
8510994
2.

Cytogenetic diagnosis of genetic diseases.

Shapiro LR, Wilmot PL.

Pediatr Ann. 1993 May;22(5):298-303. Review. No abstract available.

PMID:
8510996
3.

[Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis].

Scommegna S, Zollino M, Paolone G.

Pediatr Med Chir. 2001 May-Aug;23(3-4):191-6. Review. Italian.

PMID:
11723857
4.

Prader-Willi syndrome.

Wattendorf DJ, Muenke M.

Am Fam Physician. 2005 Sep 1;72(5):827-30. Review.

5.

[Genetic basis of Prader-Willi and Angelman syndromes: implications for the biologic diagnosis].

Dupont JM, Cuisset L.

Arch Pediatr. 1998 Apr;5(4):418-24. Review. French.

PMID:
9759164
6.

[To know more about the Prader-Willi syndrome. Diagnosis].

Midro AT, Olchowik B, Lebiedzińska A, Midro H.

Psychiatr Pol. 2009 Mar-Apr;43(2):135-49. Review. Polish.

PMID:
19697784
7.

Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.

Gilhuis HJ, van Ravenswaaij CM, Hamel BJ, Gabreëls FJ.

Eur J Paediatr Neurol. 2000;4(1):39-43. Review.

PMID:
10701104
8.

The genetics, diagnosis, and management of Prader-Willi syndrome.

Nativio DG.

J Pediatr Health Care. 2002 Nov-Dec;16(6):298-303. Review.

PMID:
12436099
9.

DNA methylation and human diseases.

El-Maarri O.

Adv Exp Med Biol. 2003;544:135-44. Review. No abstract available.

PMID:
14713224
10.

[Causes of clinical polymorphism of hereditary diseases].

Kozlova SI.

Vestn Akad Med Nauk SSSR. 1982;(6):9-13. Review. Russian. No abstract available.

PMID:
7051619
11.

[Autistic symptomatology and Prader-Willi syndrome].

Rosell-Raga L, Venegas-Venegas V.

Rev Neurol. 2006 Feb 13;42 Suppl 2:S89-93. Review. Spanish.

13.

[Prader-Willi syndrome].

Beccaria L, Bosio L, Benzi F, Bregani P, Achutegui I, Chiumello G, Livieri C, Trifirò G, de Toni T, Iughetti L, Ragusa L, Salvatoni A, Tonini G, Corrias A, Crinò A.

Ann Ist Super Sanita. 1999;35(2):221-32. Review. Italian.

PMID:
10645655
14.

Genomic imprinting relevant to genetic diseases.

Niikawa N.

Southeast Asian J Trop Med Public Health. 1997;28 Suppl 3:46-57. Review.

PMID:
9640600
15.

Genetic syndromes: from clinical suspicion to referral to diagnosis.

Shur N, Abuelo D.

Pediatr Ann. 2009 Aug;38(8):419-25. doi: 10.3928/00904481-20090723-04. Review. No abstract available.

PMID:
19711879
16.

Prader-Willi psychiatric syndrome and Velo-Cardio-Facial psychiatric syndrome.

Verhoeven WM, Tuinier S, Curfs LM.

Genet Couns. 2000;11(3):205-13. Review.

PMID:
11043428
17.

Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.

Cassidy SB, Schwartz S.

Medicine (Baltimore). 1998 Mar;77(2):140-51. Review.

PMID:
9556704
18.

What have rare genetic syndromes taught us about the pathophysiology of the common forms of obesity?

Stefan M, Nicholls RD.

Curr Diab Rep. 2004 Apr;4(2):143-50. Review.

PMID:
15035975
19.

Overview of the clinical presentation of connective tissue diseases in children.

Sills JA.

Eur J Radiol. 2000 Feb;33(2):112-7. Review. No abstract available.

PMID:
10711512
20.

Theory and practice of psychopharmacogenetics.

Tu JB.

Am J Med Genet. 1994 Dec 15;54(4):391-7. Review.

PMID:
7726214
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