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Branchio-Oculo-Facial Syndrome: Broadening the Spectrum

McCool, M.; Weaver, D. D.

American journal of medical genetics. VOL 49; NUMBER 4, ; 1994, 414 -- JOHN WILEY & SONS LTD Part: Part 4; -- 1994

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Severe Lower Limb Defects in Exstrophy of the Cloaca

Jain, M.; Weaver, D. D.

American journal of medical genetics. Part A. VOL 128; NUMB 3, ; 2004, 320-324 -- WILEY-LISS (pages 320-324) -- 2004

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Concerns about the Genetics of Pre-eclampsia

Van Meter, T. D.; Weaver, D. D.

American journal of human genetics. VOL 52; NUMBER 5, ; 1993, 1012 -- UNIVERSITY OF CHICAGO PRESS Part: Part 5; -- 1993

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Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanism

Van Meter, T. D.; Weaver, D. D.

Clinical dysmorphology. VOL 5; NUMBER 3, ; 1996, 187-196 -- CHAPMAN & HALL Part: Part 3; (pages 187-196) -- 1996

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Adults With VATER Association: Long-Term Prognosis

Wheeler, P. G.; Weaver, D. D.

American journal of medical genetics. Part A. VOL 138; NUMB 3, ; 2005, 212-217 -- WILEY-LISS (pages 212-217) -- 2005

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6
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Ramos-Arroyo syndrome: Long-term follow-up of previously reported family

Spurrier, J. L.; Weaver, D. D.

American journal of medical genetics. Part A. VOL 146; NUMBER 6, ; 2008, 675-682 -- John Wiley & Sons, Ltd (pages 675-682) -- 2008

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Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: A persistent challenge 18 years later

Escobar, L. F.; Weaver, D. D.

American journal of medical genetics. Part A. VOL 149; NUMB 5, ; 2009, 1099-1101 -- John Wiley & Sons, Ltd Part 5; (pages 1099-1101) -- 2009

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Cervical Spine Stenosis and Possible Vitamin K Deficiency Embryopathy in an Unusual Case of Chondrodysplasia Punctata and an Updated Classification System

Eash, D. D.; Weaver, D. D.; Brunetti-Pierri, N.

American journal of medical genetics. Part A. VOL 122; PART 1, ; 2003, 70-75 -- WILEY-LISS (pages 70-75) -- 2003

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Minimum Guidelines for the Delivery of Clinical Genetics Services

Weaver, D. D. et al.

American journal of human genetics. VOL 53; NUMBER 1, ; 1993, 287 -- UNIVERSITY OF CHICAGO PRESS Part: Part 1; -- 1993

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Johnson-McMillin Syndrome: Report of a New Case with Novel Features

Cushman, L. J.; Torres-Martinez, W.; Weaver, D. D.

Birth defects research. Part A, Clinical and molecular teratology. VOL 73; NUMB 9, ; 2005, 638-641 -- WILEY-LISS, INC Part: Part 9; (pages 638-641) -- 2005

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  1. Weaver, D. D.
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  5. Bull, M. J.

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