Галерея 3351909

Галерея 3351909

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Affiliation

1 Department of Pediatrics, Santa Maria Hospital, Lisbon, Portugal.

H Santos et al.

J Med Genet .

1988 Mar .

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1 Department of Pediatrics, Santa Maria Hospital, Lisbon, Portugal.

Miny P, Lenz W.
Miny P, et al.
Am J Med Genet. 1985 Jun;21(2):317-24. doi: 10.1002/ajmg.1320210214.
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PMID: 4014313

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Am J Med Genet. 1990 Jan;35(1):64-8. doi: 10.1002/ajmg.1320350112.
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PMID: 2301471

Cantwell RJ.
Cantwell RJ.
Humangenetik. 1975;26(3):261-5. doi: 10.1007/BF00281463.
Humangenetik. 1975.

PMID: 1132883

Hasegawa T, Hasegawa Y, Aso T, Koto S, Nagai T, Tsuchiya Y, Kim KC, Ohashi H, Wakui K, Fukushima Y.
Hasegawa T, et al.
Am J Med Genet. 1997 Dec 31;73(4):416-8. doi: 10.1002/(sici)1096-8628(19971231)73:4<416::aid-ajmg9>3.0.co;2-l.
Am J Med Genet. 1997.

PMID: 9415468

Review.

Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G.
Jespers A, et al.
Am J Med Genet. 1993 Aug 15;47(2):299-302. doi: 10.1002/ajmg.1320470232.
Am J Med Genet. 1993.

PMID: 8213924

Review.

Hofmann AD, Duess JW, Puri P.
Hofmann AD, et al.
Pediatr Surg Int. 2014 Aug;30(8):757-61. doi: 10.1007/s00383-014-3529-3. Epub 2014 Jun 29.
Pediatr Surg Int. 2014.

PMID: 24974188

Review.

Sepahi MA, Baraty B, Shooshtary FK.
Sepahi MA, et al.
Iran J Pediatr. 2010 Mar;20(1):123-6.
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PMID: 23056694
Free PMC article.

Moore SW.
Moore SW.
Pediatr Surg Int. 2012 Nov;28(11):1045-58. doi: 10.1007/s00383-012-3175-6. Epub 2012 Sep 23.
Pediatr Surg Int. 2012.

PMID: 23001136

Review.

Uesaka T, Nagashimada M, Yonemura S, Enomoto H.
Uesaka T, et al.
J Clin Invest. 2008 May;118(5):1890-8. doi: 10.1172/JCI34425.
J Clin Invest. 2008.

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Free PMC article.

Skinner MA, Safford SD, Reeves JG, Jackson ME, Freemerman AJ.
Skinner MA, et al.
Am J Hum Genet. 2008 Feb;82(2):344-51. doi: 10.1016/j.ajhg.2007.10.008. Epub 2008 Jan 31.
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PMID: 18252215
Free PMC article.

J Med Genet. 1973 Dec;10(4):337-9

-

PubMed

J Med Genet. 1975 Dec;12(4):334-8

-

PubMed

Pediatrics. 1985 Aug;76(2):299-300

-

PubMed

Arch Dis Child. 1983 Nov;58(11):932-3

-

PubMed

Z Kinderchir. 1982 Jan;35(1):24-5

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PubMed

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An association of Hirschsprung disease with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness is described in sibs (brother and sister) of consanguineous parents. It is suggested that this might represent a new autosomal recessive syndrome.

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Question posted by Valeriejv on 3 Dec 2017
Last updated on 3 December 2017 by PharmaGenius
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Мэдисон пришла к знаменитой массажистке но она не ожидала что в кабинете ее трахнут две лесбиянки
Галерея 3230166
Красивая и стройная задирает ножки

Галерея 3351909

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