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1
Preliminary molecular studies on blepharocheilodontic syndrome
Preliminary molecular studies on blepharocheilodontic syndrome
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Preliminary molecular studies on blepharocheilodontic syndrome

Érika L. Freitas Ciro D Martinhago; Ester Silveira Ramos; Jeffrey C Murray; Vera L Gil-da-Silva-Lopes

American Journal of Medical Genetics New York v. 143A, n. 22, p. 2757-2759, 2007

New York 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1635100 )(Acessar)

2
Preliminary molecular studies on blepharocheilodontic syndrome
Preliminary molecular studies on blepharocheilodontic syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Preliminary molecular studies on blepharocheilodontic syndrome

Érika L. Freitas Ciro D Martinhago; Ester Silveira Ramos; Jeffrey C Murray; Vera L Gil-da-Silva-Lopes

American Journal of Medical Genetics New York v. 143A, n. 22, p. 2757-2759, 2007

New York 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1635100 )(Acessar)

3
Inheritance of a CAG/CTG repeat in the HKCA3 gene in families with bipolar affective disorder
Inheritance of a CAG/CTG repeat in the HKCA3 gene in families with bipolar affective disorder
Material Type:
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Inheritance of a CAG/CTG repeat in the HKCA3 gene in families with bipolar affective disorder

I. V Meira-Lima D. A Collier; V Gentil; R. M Murray; M Gill; José Eduardo Krieger; H. P Vallada

American Journal of Medical Genetics v. 81, n. 6, p. 508-509, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

4
Inheritance of a CAG/CTG repeat in the HKCA3 gene in families with bipolar affective disorder
Inheritance of a CAG/CTG repeat in the HKCA3 gene in families with bipolar affective disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

Inheritance of a CAG/CTG repeat in the HKCA3 gene in families with bipolar affective disorder

I. V Meira-Lima D. A Collier; V Gentil; R. M Murray; M Gill; José Eduardo Krieger; H. P Vallada

American Journal of Medical Genetics v. 81, n. 6, p. 508-509, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

5
Fragile X premutation is a significant risk factor for premature ovarian failure the international collaborative POF in fragile X study - preliminary data
Fragile X premutation is a significant risk factor for premature ovarian failure the international collaborative POF in fragile X study - preliminary data
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Fragile X premutation is a significant risk factor for premature ovarian failure the international collaborative POF in fragile X study - preliminary data

Diane J Allingham-Hawkins Riyana Babul-Hirji; David Chitayat; Jeanette J A Holden; Kathy T Yang; C Lee; R Hudson; H Gorwill; Sarah L Nolin; Anne Glicksman; Edmund C Jenkins; W Ted Brown; Patricia N Howard-Peebles; Cindy Becchi; Emilie Cummings; Lee Fallon; Suzanne Seitz; Susan H Black; Angela M Vianna-Morgante; Silvia S Costa; Paulo A Otto; Regina Celia Mingroni Netto; Anna Murray; J Webb; F MacSwinney; N Dennis; Patricia A Jacobs; Maria Syrrou; Ioannis Georgiou; Phillipos C Patsalis; Maria L Giovannucci Uzielli; S Guarducci; E Lapi; A Cecconi; U Ricci; G Ricotti; C Biondi; B Scarselli; F Vieri

American Journal of Medical Genetics v. 83. n. 4, p. 322-325, apr., 1999

New York 1999

Item não circula. Consulte sua biblioteca.(Acessar)

6
Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome
Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome
Material Type:
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Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome

Ferreira de Lima, R.L.L. ; Moretti-Ferreira, D. ; Richieri-Costa, A. ; Murray, J.C.

American journal of medical genetics, 2003-09, Vol.122A (1), p.56-58 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Prenatal diagnosis is for the DR, not just for the OR
Prenatal diagnosis is for the DR, not just for the OR
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Prenatal diagnosis is for the DR, not just for the OR

Murray, Jeffrey C.

American journal of medical genetics, 2003-08, Vol.120A (4), p.594-595 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome
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Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome

Schutte, Brian C. ; Basart, Ann M. ; Watanabe, Yoriko ; Laffin, Jennifer J.S. ; Coppage, Kevin ; Bjork, Bryan C. ; Daack-Hirsch, Sandy ; Patil, Shiva ; Dixon, Michael J. ; Murray, Jeffrey C.

American journal of medical genetics, 1999-05, Vol.84 (2), p.145-150

New York: Wiley Subscription Services, Inc., A Wiley Company

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9
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome
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Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome

Lin, Angela E. ; Semina, Elena V. ; Daack-Hirsch, Sandra ; Roeder, Elizabeth R. ; Curry, Cynthia J.R. ; Rosenbaum, Kenneth ; Weaver, David D. ; Murray, Jeffrey C.

American journal of medical genetics, 2000-04, Vol.91 (5), p.387-390

New York: John Wiley & Sons, Inc

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10
Linkage localization of Börjeson-Forssman-Lehmann syndrome
Linkage localization of Börjeson-Forssman-Lehmann syndrome
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Linkage localization of Börjeson-Forssman-Lehmann syndrome

Mathews, Katherine D. ; Ardinger, Holly H. ; Nishimura, Darryl Y. ; Buetow, Kenneth H. ; Murray, Jeffrey C. ; Bartley, James A.

American journal of medical genetics, 1989-12, Vol.34 (4), p.470-474

New York: Wiley Subscription Services, Inc., A Wiley Company

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Deste Autor:

  1. Murray, R
  2. Gentil, V
  3. Ramos, E
  4. Meira-Lima, I
  5. Gill, M

Neste Assunto:

  1. Medical Sciences
  2. Biological And Medical Sciences
  3. Humans
  4. Genetics & Heredity
  5. Life Sciences & Biomedicine

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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